Riboflavin Intron Data


Gene SymbolChromosomeStartEndrs IDStrandNCBI refObservedClassFunctionSubmitter CountSubmitterFrequency CountAllele Frequency
NDUFV1chr116737883767378838rs2306144+CA/C/Gsingleintron51000GENOMES,NHLBI-ESP,RIKENSNPRC,SSMP,YUSUKE,20.957354
NDUFV1chr116737907867379079rs112015076+GC/Gsingleintron51000GENOMES,BUSHMAN,ILLUMINA,NHLBI-ESP,TISHKOFF,20.013761
NDUFV1chr116737957467379575rs12295232+GA/Gsingleintron,near-gene-561000GENOMES,BUSHMAN,ILLUMINA,KRIBB_YJKIM,SC_SNP,TISHKOFF,20.052808
NDUFV1chr116737976267379763rs4148958+GA/Gsingleintron,near-gene-551000GENOMES,BGI,GMI,RIKENSNPRC,SSMP,20.010393
ACADSchr12121164489121164490rs11065229+CA/Csingleintron91000GENOMES,AFFY,BGI,BUSHMAN,GMI,ILLUMINA,KRIBB_YJKIM,SC_SNP,SSMP,20.082822
ACADSchr12121164651121164652rs11065230+CC/Tsingleintron151000GENOMES,ABI,BCM-HGSC-SUB,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,ILLUMINA,ILLUMINA-UK,IMCJ-GDT,PERLEGEN,PJP,SC_SNP,SSMP,TISHKOFF,20.873597
ACADSchr12121165317121165318rs77596870+GA/Gsingleintron41000GENOMES,COMPLETE_GENOMICS,ILLUMINA,SSMP,20.022477
ACADSchr12121165812121165813rs148642194+CC/Tsingleintron21000GENOMES,TISHKOFF,20.987144
ACADSchr12121166162121166163rs61239175+CC/Tsingleintron51000GENOMES,GMI,HGSV,ILLUMINA,SSMP,20.953438
ACADSchr12121166454121166455rs61624288+GA/Gsingleintron71000GENOMES,BUSHMAN,COMPLETE_GENOMICS,GMI,HGSV,SSMP,TISHKOFF,20.029331
ACADSchr12121167038121167039rs7978125+AA/Gsingleintron191000GENOMES,ABI,BCM-HGSC-SUB,BGI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PJP,SC_SNP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.475193
ACADSchr12121167195121167196rs12425598+TC/Tsingleintron41000GENOMES,ABI,CSHL-HAPMAP,ENSEMBL,20.023853
ACADSchr12121167386121167387rs3999408-CA/Gsingleintron141000GENOMES,ABI,BUSHMAN,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,PERLEGEN,PJP,SC_JCM,SSMP,TISHKOFF,TSC-CSHL,20.198471
ACADSchr12121167743121167744rs10849781+CA/Csingleintron101000GENOMES,AFFY,BGI,CSHL-HAPMAP,GMI,ILLUMINA,KRIBB_YJKIM,PJP,SC_SNP,SSMP,20.088599
ACADSchr12121168030121168031rs111999968+GA/Gsingleintron31000GENOMES,COMPLETE_GENOMICS,SSMP,20.034404
ACADSchr12121168072121168073rs3794216-CC/Gsingleintron31000GENOMES,SSMP,YUSUKE,20.022039
ACADSchr12121168082121168083rs3794215-TA/Gsingleintron191000GENOMES,ABI,BCM-HGSC-SUB,BCM_SSAHASNP,BGI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PJP,SC_SNP,SSAHASNP,SSMP,TISHKOFF,YUSUKE,20.468582
ACADSchr12121168244121168245rs3794214-TA/Gsingleintron201000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BCM_SSAHASNP,BGI,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SC_SNP,SSAHASNP,SSMP,TISHKOFF,YUSUKE,20.448314
ACADSchr12121168570121168571rs150146692+CC/Tsingleintron21000GENOMES,TISHKOFF,20.989899
ACADSchr12121168602121168602rs3838807---/CAinsertionintron71000GENOMES,ABI,BILGI_BIOE,DEVINE_LAB,GMI,LUNTER,YUSUKE,20.388430
ACADSchr12121168603121168603rs63009860+--/GC/GT/TGinsertionintron61000GENOMES,DEVINE_LAB,HUMANGENOME_JCVI,PJP,SSMP,TISHKOFF,20.412844
ACADSchr12121168616121168617rs75148250+TC/Tsingleintron21000GENOMES,ILLUMINA,20.010453
ACADSchr12121169355121169356rs11065231+CA/Csingleintron121000GENOMES,ABI,BCM-HGSC-SUB,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SC_SNP,SSMP,20.520567
ACADSchr12121169435121169436rs696339-AA/Tsingleintron131000GENOMES,ABI,BCM-HGSC-SUB,BUSHMAN,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA-UK,KWOK,PJP,SC_SNP,SSAHASNP,SSMP,20.598627
ACADSchr12121170094121170095rs11065232+CA/Csingleintron31000GENOMES,SC_SNP,SSMP,20.127181
ACADSchr12121170256121170257rs34346357+TC/Tsingleintron61000GENOMES,ABI,HGSV,HUMANGENOME_JCVI,PJP,SSMP,20.369266
ACADSchr12121170271121170272rs11065233+TC/Tsingleintron71000GENOMES,ABI,HGSV,HUMANGENOME_JCVI,PJP,SC_SNP,SSMP,20.485780
ACADSchr12121170338121170339rs34491494+CC/Tsingleintron71000GENOMES,ABI,GMI,HGSV,HUMANGENOME_JCVI,PJP,SSMP,20.604950
ACADSchr12121170345121170346rs148589034+GA/Gsingleintron21000GENOMES,SSMP,20.027089
ACADSchr12121170637121170638rs190188111+AA/Gsingleintron11000GENOMES,20.952250
ACADSchr12121171036121171037rs113979967+GG/Tsingleintron51000GENOMES,BUSHMAN,COMPLETE_GENOMICS,GMI,TISHKOFF,20.974794
ACADSchr12121171059121171060rs11065234+GA/Gsingleintron41000GENOMES,BGI,GMI,SC_SNP,20.077594
ACADSchr12121171236121171237rs708781-GC/Tsingleintron41000GENOMES,ILLUMINA,KWOK,TSC-CSHL,20.979835
ACADSchr12121171338121171353rs67132258+TGCCTGCTGAAATGGlengthTooLongin-delintron,cds-indel31000GENOMES,DEVINE_LAB,LUNTER,20.612489
ACADSchr12121171802121171803rs558314-CC/Gsingleintron211000GENOMES,ABI,BCM-HGSC-SUB,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KWOK,PJP,SC_JCM,SC_SNP,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.732453
ACADSchr12121171887121171888rs12368617+GA/Gsingleintron61000GENOMES,COMPLETE_GENOMICS,GMI,ILLUMINA,SC_SNP,SSMP,20.013761
ACADSchr12121171890121171891rs34673751+GA/Gsingleintron111000GENOMES,ABI,BGI,BUSHMAN,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA,PJP,SSMP,TISHKOFF,20.184355
ACADSchr12121172222121172223rs7957395+GA/Gsingleintron31000GENOMES,ILLUMINA,WI_SSAHASNP,20.010889
ACADSchr12121172265121172266rs11065235+CC/Tsingleintron81000GENOMES,AFFY,BGI,GMI,ILLUMINA,KRIBB_YJKIM,SC_SNP,SSMP,20.915943
ACADSchr12121172921121172922rs148270270+AA/Tsingleintron21000GENOMES,TISHKOFF,20.972911
ACADSchr12121173030121173031rs7312316+TC/Tsingleintron61000GENOMES,BCM-HGSC-SUB,BCM_SSAHASNP,ENSEMBL,GMI,SSMP,20.538038
ACADSchr12121173100121173104rs144390141+AAAC-/AAACdeletionintron31000GENOMES,LUNTER,SSMP,20.122590
ACADSchr12121173162121173162rs201595000+--/Cinsertionintron11000GENOMES,20.926997
ACADSchr12121173385121173386rs56232241+TC/Tsingleintron41000GENOMES,BCM-HGSC-SUB,HGSV,TISHKOFF,20.033507
ACADSchr12121173430121173431rs575437+TC/Tsingleintron181000GENOMES,ABI,BCM-HGSC-SUB,BCM_SSAHASNP,BUSHMAN,COMPLETE_GENOMICS,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KWOK,PJP,SC_JCM,SC_SNP,SSAHASNP,SSMP,TISHKOFF,20.551598
ACADSchr12121173652121173653rs696340+AA/Tsingleintron171000GENOMES,ABI,BCM-HGSC-SUB,BGI,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,KWOK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.526916
ACADSchr12121173751121173752rs80005880+AA/Gsingleintron31000GENOMES,ILLUMINA,TISHKOFF,20.945557
ACADSchr12121173798121173816rs201057576+TCCCTGTCCCCGTCC-/TCCCTGTCCCCGTdeletionintron21000GENOMES,LUNTER,20.021579
ACADSchr12121173809121173815rs146046379+GTCCCT-/GTCCCTdeletionintron21000GENOMES,LUNTER,20.047750
ACADSchr12121173827121173833rs200960176+GTCCCT-/GTCCCTdeletionintron11000GENOMES,20.021579
ACADSchr12121173931121173932rs708783+AA/Gsingleintron131000GENOMES,ABI,BCM-HGSC-SUB,BGI,BUSHMAN,COMPLETE_GENOMICS,GMI,HGSV,ILLUMINA-UK,KWOK,PJP,SC_JCM,SSMP,20.384369
ACADSchr12121173973121173973rs59063082+--/Ginsertionintron81000GENOMES,BILGI_BIOE,BUSHMAN,GMI,HGSV,LUNTER,SSMP,TISHKOFF,20.734404
ACADSchr12121174312121174313rs115132997+AA/Gsingleintron31000GENOMES,ILLUMINA,TISHKOFF,20.961237
ACADSchr12121174764121174765rs112669327+CC/Tsingleintron51000GENOMES,BUSHMAN,ILLUMINA,NHLBI-ESP,TISHKOFF,20.972477
ACADSchr12121175484121175485rs2239687+CA/Csingleintron51000GENOMES,GMI,SC_SNP,SSMP,YUSUKE,20.084856
ACADSchr12121175490121175491rs12231499+TG/Tsingleintron51000GENOMES,GMI,IMCJ-GDT,SC_SNP,SSMP,20.077452
ACADSchr12121175523121175524rs2014355+TC/Tsingleintron131000GENOMES,ABI,AFFY,BGI,BUSHMAN,EXOME_CHIP,GMI,HUMANGENOME_JCVI,KRIBB_YJKIM,PERLEGEN,SSMP,TISHKOFF,TSC-CSHL,20.164092
ACADSchr12121175559121175560rs695950-GC/Gsingleintron161000GENOMES,ABI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,GMI,HGSV,ILLUMINA,ILLUMINA-UK,KWOK,PERLEGEN,PJP,SC_JCM,SSMP,TISHKOFF,TSC-CSHL,20.778677
ACADSchr12121175561121175562rs117636828+GA/Gsingleintron21000GENOMES,SSMP,20.023064
ACADSchr12121175609121175610rs117000908+GA/Gsingleintron51000GENOMES,CLINSEQ_SNP,ILLUMINA,NHLBI-ESP,SSMP,20.021035
ACADSchr12121175983121175984rs555404+TC/Tsingleintron221000GENOMES,ABI,BCM-HGSC-SUB,BGI,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,KWOK,PERLEGEN,PJP,SC_JCM,SC_SNP,SSMP,TISHKOFF,TSC-CSHL,YUSUKE,20.567517
ACADSchr12121176292121176293rs17848090+CC/Tsingleintron61000GENOMES,BGI,CLINSEQ_SNP,IMCJ-GDT,NHLBI-ESP,SSMP,20.934360
ACADSchr12121176548121176549rs487915+CC/Tsingleintron111000GENOMES,ABI,CSHL-HAPMAP,ENSEMBL,GMI,ILLUMINA,IMCJ-GDT,KWOK,SC_JCM,SSMP,YUSUKE,20.916209
ACADSchr12121176769121176770rs2071266+CC/Tsingleintron81000GENOMES,BGI,GMI,HGBASE,IMCJ-GDT,NHLBI-ESP,SSMP,YUSUKE,20.922936
ACADSchr12121176803121176803rs57852948+--/Cinsertionintron81000GENOMES,DEVINE_LAB,GMI,HGSV,LUNTER,PJP,SSMP,TISHKOFF,20.882461
ACADSchr12121176901121176902rs140372512+GA/Gsingleintron51000GENOMES,CLINSEQ_SNP,NHLBI-ESP,SSMP,WARNICH_LAB,20.015353
COQ6chr147441666474416665rs17094157+TC/Tsingleintron,near-gene-5,untranslated-591000GENOMES,BUSHMAN,CLINSEQ_SNP,GMI,ILLUMINA,KYUGEN,NHLBI-ESP,PERLEGEN,SSMP,30.084197
COQ6chr147441693674416937rs17094164+GC/Gsingleintron,near-gene-5,untranslated-531000GENOMES,PERLEGEN,TISHKOFF,20.013603
COQ6chr147441694474416945rs17552038+GC/Gsingleintron,near-gene-5,untranslated-5121000GENOMES,ABI,BCM-HGSC-SUB,BL,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,KYUGEN,PJP,SI_EXO,SSMP,20.107045
COQ6chr147441699574416996rs78801603+GG/Tsingleintron,untranslated-531000GENOMES,ILLUMINA,NHLBI-ESP,20.972561
COQ6chr147441720874417209rs60369619+CC/Tsingleintron,near-gene-561000GENOMES,BUSHMAN,HGSV,ILLUMINA,NHLBI-ESP,TISHKOFF,20.984876
COQ6chr147441748774417488rs76260393+TC/Tsingleintron,near-gene-521000GENOMES,TISHKOFF,20.016986
COQ6chr147441755474417555rs112218167+TG/Tsingleintron,near-gene-531000GENOMES,COMPLETE_GENOMICS,ILLUMINA,20.051376
COQ6chr147441759774417598rs11850082+CA/Csingleintron,near-gene-541000GENOMES,ABI,CSHL-HAPMAP,ENSEMBL,20.014207
COQ6chr147441760874417609rs59892091+TC/Tsingleintron,near-gene-541000GENOMES,GMI,HGSV,SSMP,20.090157
COQ6chr147441764974417650rs11850094+CC/Tsingleintron,near-gene-541000GENOMES,ABI,CSHL-HAPMAP,ENSEMBL,20.979167
COQ6chr147441771174417712rs11850097+AA/Gsingleintron,near-gene-541000GENOMES,ABI,CSHL-HAPMAP,ENSEMBL,20.988543
COQ6chr147441779774417798rs8013496+GC/Gsingleintron,near-gene-5131000GENOMES,ABI,BCMHGSC_JDW,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,PJP,SSMP,TISHKOFF,WI_SSAHASNP,20.363969
COQ6chr147441791274417913rs112260439+GG/Tsingleintron,near-gene-531000GENOMES,BUSHMAN,TISHKOFF,20.985780
COQ6chr147441806574418066rs114383382+GC/Gsingleintron,near-gene-521000GENOMES,TISHKOFF,20.013937
COQ6chr147441814074418141rs11628276+GA/Gsingleintron,near-gene-5101000GENOMES,ABI,BCMHGSC_JDW,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,PJP,SSMP,TISHKOFF,20.248856
COQ6chr147441858774418588rs66712197+GA/Gsingleintron,near-gene-581000GENOMES,BCM-HGSC-SUB,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SSMP,20.105769
COQ6chr147441874974418750rs72723772+TC/Tsingleintron,near-gene-531000GENOMES,GMI,SSMP,20.021120
COQ6chr147441896974418970rs77680522+CC/Tsingleintron,near-gene-551000GENOMES,BGI,GMI,SSMP,TISHKOFF,20.859045
COQ6chr147441919074419191rs10459544+CC/Gsingleintron151000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SC_SNP,SSAHASNP,SSMP,TISHKOFF,20.164765
COQ6chr147441920874419209rs10459545+AA/Gsingleintron181000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA,PJP,SC_SNP,SSAHASNP,SSMP,TISHKOFF,20.339100
COQ6chr147441924574419246rs191928320+AA/Tsingleintron11000GENOMES,20.989440
COQ6chr147441924674419247rs10459546+AA/Tsingleintron101000GENOMES,ABI,BL,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SC_SNP,SSMP,20.881410
COQ6chr147441935474419355rs111553135+CC/Tsingleintron31000GENOMES,BUSHMAN,TISHKOFF,20.968349
COQ6chr147441952674419527rs141219050+CC/Tsingleintron11000GENOMES,20.986226
COQ6chr147441964174419642rs10459547+GG/Tsingleintron111000GENOMES,BCM-HGSC-SUB,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SC_SNP,SSAHASNP,SSMP,20.892955
COQ6chr147441982474419825rs4903159+GA/Gsingleintron181000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.659893
COQ6chr147442002974420030rs112742205+TC/Tsingleintron31000GENOMES,COMPLETE_GENOMICS,ILLUMINA,20.018807
COQ6chr147442010874420109rs60157646+TG/Tsingleintron81000GENOMES,BUSHMAN,CLINSEQ_SNP,HGSV,ILLUMINA,ILLUMINA-UK,NHLBI-ESP,TISHKOFF,20.022334
COQ6chr147442012674420127rs3213692-CA/Gsingleintron131000GENOMES,BCM-HGSC-SUB,BGI,CLINSEQ_SNP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,NHLBI-ESP,PJP,SSAHASNP,SSMP,YUSUKE,20.238280
COQ6chr147442012674420127rs200558787+C-/Cdeletionintron11000GENOMES,20.216253
COQ6chr147442043974420440rs17094182+CA/Csingleintron91000GENOMES,AFFY,BGI,GMI,ILLUMINA,KRIBB_YJKIM,PERLEGEN,SSMP,TISHKOFF,20.161667
COQ6chr147442052474420527rs143983947+TGT-/TGTdeletionintron41000GENOMES,BL,GMI,LUNTER,20.050046
COQ6chr147442062074420620rs146800451+--/AGinsertionintron31000GENOMES,GMI,LUNTER,20.915519
COQ6chr147442092174420922rs11629101+TC/Tsingleintron81000GENOMES,ABI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,GMI,SSMP,TISHKOFF,20.342159
COQ6chr147442114974421152rs200188951+AAC-/AACdeletionintron21000GENOMES,LUNTER,20.013774
COQ6chr147442121174421212rs2079632-CC/Gsingleintron161000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SC_JCM,SSAHASNP,SSMP,TSC-CSHL,WI_SSAHASNP,20.873028
COQ6chr147442132074421321rs2098030-CA/Gsingleintron101000GENOMES,ABI,BCM-HGSC-SUB,BL,COMPLETE_GENOMICS,ENSEMBL,SC_JCM,SSAHASNP,SSMP,TSC-CSHL,20.103022
COQ6chr147442137574421376rs140936556+CA/Csingleintron21000GENOMES,TISHKOFF,20.013774
COQ6chr147442141174421412rs117895742+CC/Tsingleintron11000GENOMES,20.977372
COQ6chr147442153274421533rs150260008+CC/Tsingleintron21000GENOMES,SSMP,20.769054
COQ6chr147442154174421542rs139022996+GA/Gsingleintron21000GENOMES,GMI,20.328283
COQ6chr147442156574421566rs191731397+TA/Tsingleintron21000GENOMES,GMI,20.248852
COQ6chr147442156574421566rs201876533+T-/Tdeletionintron11000GENOMES,20.241506
COQ6chr147442162574421626rs115919509+AA/Gsingleintron21000GENOMES,TISHKOFF,20.970819
COQ6chr147442164674421647rs113358234+TA/Tsingleintron41000GENOMES,BUSHMAN,COMPLETE_GENOMICS,GMI,20.351971
COQ6chr147442166174421662rs188075790+TA/Tsingleintron11000GENOMES,20.046373
COQ6chr147442168074421681rs189541577+GG/Tsingleintron21000GENOMES,TISHKOFF,20.970156
COQ6chr147442232874422329rs2302118-GC/Gsingleintron141000GENOMES,ABI,BCMHGSC_JDW,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,YUSUKE,20.812666
COQ6chr147442238574422386rs75531541+CC/Tsingleintron21000GENOMES,ILLUMINA,20.980418
COQ6chr147442280174422802rs188395141+CC/Tsingleintron21000GENOMES,SSMP,20.977043
COQ6chr147442280274422803rs112488013+GA/Gsingleintron41000GENOMES,BUSHMAN,COMPLETE_GENOMICS,TISHKOFF,20.025618
COQ6chr147442284274422843rs1972538-TA/Gsingleintron101000GENOMES,ABI,COMPLETE_GENOMICS,ENSEMBL,GMI,PJP,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.778185
COQ6chr147442285374422854rs113608012+TC/Tsingleintron31000GENOMES,COMPLETE_GENOMICS,SSMP,20.011009
COQ6chr147442290374422904rs112175736+GA/Gsingleintron31000GENOMES,BUSHMAN,TISHKOFF,20.018781
COQ6chr147442292274422923rs1985969-TA/Gsingleintron161000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,PJP,SC_SNP,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.526484
COQ6chr147442321774423218rs10148057+CC/Tsingleintron31000GENOMES,ILLUMINA,WI_SSAHASNP,20.983821
COQ6chr147442335674423363rs143222231+TCCACTT-/TCCACTTdeletionintron41000GENOMES,GMI,LUNTER,PJP,20.327365
COQ6chr147442351774423518rs75446133+CC/Tsingleintron11000GENOMES,20.986498
COQ6chr147442365874423659rs11623965+TC/Tsingleintron71000GENOMES,ABI,BCMHGSC_JDW,CSHL-HAPMAP,ENSEMBL,GMI,SSMP,20.235133
COQ6chr147442378174423782rs11850995+CC/Tsingleintron71000GENOMES,ABI,AFFY,CSHL-HAPMAP,ENSEMBL,ILLUMINA,KRIBB_YJKIM,20.977887
COQ6chr147442380074423801rs181739324+AA/Tsingleintron21000GENOMES,GMI,20.943526
COQ6chr147442380374423804rs4903160+AA/Tsingleintron51000GENOMES,CSHL-HAPMAP,ENSEMBL,GMI,WI_SSAHASNP,20.719523
COQ6chr147442380374423804rs200787774+A-/Adeletionintron21000GENOMES,SSMP,20.280533
COQ6chr147442380574423805rs201739413+--/TAinsertionintron11000GENOMES,20.797521
COQ6chr147442380674423806rs199572425+--/Ainsertionintron21000GENOMES,GMI,20.797980
COQ6chr147442383674423837rs60611458+GA/Gsingleintron41000GENOMES,COMPLETE_GENOMICS,HGSV,TISHKOFF,20.022477
COQ6chr147442395574423956rs62006130+GA/Gsingleintron71000GENOMES,BCMHGSC_JDW,BUSHMAN,ENSEMBL,GMI,SSMP,TISHKOFF,20.318515
COQ6chr147442420174424202rs77803340+GA/Gsingleintron21000GENOMES,TISHKOFF,20.029617
COQ6chr147442425874424259rs114800916+GG/Tsingleintron21000GENOMES,TISHKOFF,20.984756
COQ6chr147442426474424265rs62006131+TA/C/Tsingleintron81000GENOMES,BCMHGSC_JDW,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,SSMP,TISHKOFF,20.345995
COQ6chr147442449074424491rs17782310+TC/Tsingleintron71000GENOMES,BCMHGSC_JDW,ENSEMBL,GMI,PERLEGEN,SSMP,TISHKOFF,20.222653
COQ6chr147442454374424544rs79537722+GA/Gsingleintron21000GENOMES,TISHKOFF,20.014373
COQ6chr147442474074424741rs10151933+GA/Gsingleintron31000GENOMES,ILLUMINA,WI_SSAHASNP,20.012722
COQ6chr147442505574425056rs3764859-CG/Tsingleintron191000GENOMES,ABI,AFFY,BCMHGSC_JDW,BCM_SSAHASNP,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA,KRIBB_YJKIM,PERLEGEN,PJP,SI_EXO,SSMP,TISHKOFF,YUSUKE,20.679628
COQ6chr147442631374426314rs57268226+AA/Gsingleintron31000GENOMES,HGSV,TISHKOFF,20.985192
COQ6chr147442637474426375rs145747095+CC/Tsingleintron31000GENOMES,GMI,SSMP,20.914141
COQ6chr147442667174426672rs2072291-CA/Gsingleintron221000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGBASE,HGSV,HUMANGENOME_JCVI,KRIBB_YJKIM,PJP,SSAHASNP,SSMP,TISHKOFF,YUSUKE,20.614831
COQ6chr147442685374426854rs740505+TC/Tsingleintron151000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BL,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,PJP,SSMP,TISHKOFF,TSC-CSHL,20.139264
COQ6chr147442692974426930rs740504+AA/Gsingleintron131000GENOMES,ABI,BCM-HGSC-SUB,BL,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SSMP,TISHKOFF,TSC-CSHL,20.856322
COQ6chr147442694174426942rs10873263+AA/Csingleintron111000GENOMES,ABI,AFFY,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,KRIBB_YJKIM,PJP,SSMP,TISHKOFF,20.808896
COQ6chr147442697074426971rs34468446+AA/Gsingleintron91000GENOMES,ABI,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SSMP,TISHKOFF,20.879689
COQ6chr147442740474427405rs2098029-CA/Gsingleintron111000GENOMES,ABI,BCM-HGSC-SUB,BL,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SSMP,TSC-CSHL,20.090577
COQ6chr147442740574427406rs115579294+GA/Gsingleintron41000GENOMES,ILLUMINA,SSMP,TISHKOFF,20.010889
COQ6chr147442762474427625rs75088275+GC/Gsingleintron11000GENOMES,20.015244
COQ6chr147442767374427674rs79246780+CC/Tsingleintron21000GENOMES,ILLUMINA,20.974325
COQ6chr147442828574428286rs7141392+AA/Gsingleintron181000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,ENSEMBL,GMI,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PJP,SSAHASNP,SSMP,TISHKOFF,20.145259
COQ6chr147442833774428338rs116737018+CC/Tsingleintron21000GENOMES,TISHKOFF,20.984756
COQ6chr147442885074428851rs12880050+AA/Gsingleintron111000GENOMES,ABI,BCM-HGSC-SUB,BL,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SSAHASNP,SSMP,20.899360
COQ6chr147442909074429091rs72627141+TC/Tsingleintron61000GENOMES,BGI,GMI,ILLUMINA,SSMP,TISHKOFF,20.153391
COQ6chr147442912474429125rs113145643+GA/Gsingleintron31000GENOMES,COMPLETE_GENOMICS,TISHKOFF,20.022018
COQ6chr147442913274429133rs7147088+AA/Gsingleintron111000GENOMES,ABI,BCMHGSC_JDW,BCM_SSAHASNP,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,SSMP,TISHKOFF,20.653705
COQ6chr147442913674429137rs7147229+CC/Gsingleintron101000GENOMES,ABI,BCMHGSC_JDW,BCM_SSAHASNP,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,SSMP,TISHKOFF,20.765811
COQ6chr147442940974429411rs57794133+TA-/TAdeletionintron131000GENOMES,BCMHGSC_JDW,BILGI_BIOE,BL,BUSHMAN,DEVINE_LAB,GMI,HGSV,HUMANGENOME_JCVI,LUNTER,PJP,SSMP,TISHKOFF,20.614011
COQ6chr147442941274429413rs200726437+A-/Adeletionintron11000GENOMES,20.271809
L2HGDHchr145071412850714129rs17122318+AA/Gsingleintron31000GENOMES,PERLEGEN,TISHKOFF,20.969298
L2HGDHchr145071418050714181rs143645778+AA/Gsingleintron11000GENOMES,20.988062
L2HGDHchr145071419350714194rs737077+CC/Tsingleintron141000GENOMES,ABI,AFFY,BUSHMAN,COMPLETE_GENOMICS,GMI,HGSV,ILLUMINA,KRIBB_YJKIM,PERLEGEN,PJP,SSMP,TISHKOFF,TSC-CSHL,20.673541
L2HGDHchr145071427350714274rs737078+CC/Tsingleintron221000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SSAHASNP,SSMP,TSC-CSHL,WI_SSAHASNP,20.456721
L2HGDHchr145071433150714332rs737079+CA/Csingleintron121000GENOMES,ABI,BGI,BUSHMAN,COMPLETE_GENOMICS,GMI,HGSV,ILLUMINA,PJP,SSMP,TSC-CSHL,WI_SSAHASNP,20.328963
L2HGDHchr145071471150714712rs761817+TC/Tsingleintron191000GENOMES,ABI,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TSC-CSHL,WI_SSAHASNP,20.908801
L2HGDHchr145071498450714985rs743075-TA/Gsingleintron221000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.451149
L2HGDHchr145071499250714993rs79961648+AA/Csingleintron21000GENOMES,TISHKOFF,20.963415
L2HGDHchr145071521850715219rs743076+AA/Gsingleintron111000GENOMES,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,GMI,ILLUMINA,KRIBB_YJKIM,SSMP,TISHKOFF,TSC-CSHL,20.714386
L2HGDHchr145071527450715275rs74699989+CA/Csingleintron21000GENOMES,ILLUMINA,20.010453
L2HGDHchr145071556350715564rs7155191+TC/Tsingleintron131000GENOMES,ABI,BCM_SSAHASNP,BGI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,PJP,SSMP,TISHKOFF,WI_SSAHASNP,20.330137
L2HGDHchr145071564150715642rs10136539+CC/Tsingleintron121000GENOMES,ABI,BGI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,ILLUMINA,SSMP,TISHKOFF,WI_SSAHASNP,20.688563
L2HGDHchr145071586150715862rs2092897+TC/Tsingleintron5ABI,ILLUMINA,KRIBB_YJKIM,SC_JCM,TSC-CSHL,20.422053
L2HGDHchr145071626550716266rs67871518+CC/Tsingleintron71000GENOMES,BGI,BUSHMAN,COMPLETE_GENOMICS,GMI,SSMP,TISHKOFF,20.674908
L2HGDHchr145071628750716288rs66726816+CC/Tsingleintron71000GENOMES,BGI,BUSHMAN,COMPLETE_GENOMICS,GMI,SSMP,TISHKOFF,20.674908
L2HGDHchr145071657750716578rs73275103+CC/Tsingleintron81000GENOMES,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,GMI,SSMP,TISHKOFF,20.725149
L2HGDHchr145071664950716650rs61982731+CC/Tsingleintron91000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SSMP,TISHKOFF,20.747021
L2HGDHchr145071739350717394rs80343828+CC/Gsingleintron11000GENOMES,20.989547
L2HGDHchr145071744750717448rs4901002+GC/Gsingleintron191000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.583090
L2HGDHchr145071872050718721rs57075287+TC/Tsingleintron31000GENOMES,HGSV,TISHKOFF,20.036150
L2HGDHchr145071900150719002rs11628216+CC/Tsingleintron151000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,GMI,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,20.128545
L2HGDHchr145071907450719075rs140009986+AA/Csingleintron11000GENOMES,20.979798
L2HGDHchr145071921350719214rs76691238+A-/Adeletionintron61000GENOMES,BGI,GMI,LUNTER,SSMP,TISHKOFF,20.320478
L2HGDHchr145071925950719260rs11628296+CC/Tsingleintron151000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,20.741112
L2HGDHchr145071961450719615rs10149715+GA/Gsingleintron101000GENOMES,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,PJP,SSMP,TISHKOFF,WI_SSAHASNP,20.332310
L2HGDHchr145071982750719828rs12893979+CC/Tsingleintron131000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BUSHMAN,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,20.742216
L2HGDHchr145072006150720062rs7152434+TA/Tsingleintron81000GENOMES,BCM_SSAHASNP,COMPLETE_GENOMICS,GMI,PJP,SSMP,TISHKOFF,WI_SSAHASNP,20.331044
L2HGDHchr145072020450720205rs7151353+CC/Tsingleintron171000GENOMES,ABI,BCMHGSC_JDW,BCM_SSAHASNP,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.091158
L2HGDHchr145072028450720285rs7151371+AA/Csingleintron141000GENOMES,ABI,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.050459
L2HGDHchr145072029450720295rs114504167+CA/Csingleintron51000GENOMES,BL,GMI,SSMP,TISHKOFF,20.263013
L2HGDHchr145072091150720912rs12890974+TC/Tsingleintron121000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BUSHMAN,GMI,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,20.260385
L2HGDHchr145072126550721266rs56075103+AA/Gsingleintron41000GENOMES,HGSV,ILLUMINA,SSMP,20.976066
L2HGDHchr145072159650721596rs201706273+--/Ainsertionintron11000GENOMES,20.968320
L2HGDHchr145072169350721694rs76152450+GA/Gsingleintron21000GENOMES,TISHKOFF,20.034843
L2HGDHchr145072194650721947rs56357220+AA/Gsingleintron31000GENOMES,HGSV,ILLUMINA-UK,20.988991
L2HGDHchr145072200950722010rs72683914+CC/Tsingleintron41000GENOMES,COMPLETE_GENOMICS,SSMP,TISHKOFF,20.874771
L2HGDHchr145072215050722151rs144943179+GA/Gsingleintron31000GENOMES,GMI,SSMP,20.014233
L2HGDHchr145072235850722359rs8004803+AA/Csingleintron201000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.447311
L2HGDHchr145072266350722664rs2013330+TC/Tsingleintron61000GENOMES,GMI,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.299007
L2HGDHchr145072269150722692rs61553770+GC/Gsingleintron31000GENOMES,HGSV,TISHKOFF,20.010560
L2HGDHchr145072285350722854rs79624057+CC/Tsingleintron21000GENOMES,TISHKOFF,20.988240
L2HGDHchr145072293750722938rs141938219+AA/Gsingleintron11000GENOMES,20.989899
L2HGDHchr145072328450723285rs910640+TA/Tsingleintron211000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.870776
L2HGDHchr145072328550723285rs201497484+--/Ainsertionintron11000GENOMES,20.328283
L2HGDHchr145072363050723631rs4901004+TC/Tsingleintron81000GENOMES,BUSHMAN,COMPLETE_GENOMICS,ILLUMINA,PERLEGEN,SSMP,TISHKOFF,WI_SSAHASNP,20.125000
L2HGDHchr145072395950723960rs910641+TC/Tsingleintron231000GENOMES,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PERLEGEN,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.862675
L2HGDHchr145072433750724338rs2007750+GC/Gsingleintron191000GENOMES,ABI,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PJP,SC_SNP,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.910210
L2HGDHchr145072457250724573rs77076798+AA/Gsingleintron21000GENOMES,TISHKOFF,20.974739
L2HGDHchr145072508550725086rs10151271+AA/Tsingleintron111000GENOMES,ABI,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,PJP,SSMP,TISHKOFF,WI_SSAHASNP,20.666362
L2HGDHchr145072577250725773rs10151883+AA/Gsingleintron201000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.121923
L2HGDHchr145072597950725980rs76712673+CA/Csingleintron11000GENOMES,20.010453
L2HGDHchr145072607650726076rs201690350+--/Tinsertionintron11000GENOMES,20.625803
L2HGDHchr145072621850726219rs112396161+CC/Tsingleintron21000GENOMES,COMPLETE_GENOMICS,20.983028
L2HGDHchr145072623450726235rs28785597+GA/Gsingleintron81000GENOMES,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,GMI,SSAHASNP,SSMP,20.329821
L2HGDHchr145072627850726279rs150919319+GA/Gsingleintron11000GENOMES,20.010560
L2HGDHchr145072630350726304rs11849315+TC/Tsingleintron151000GENOMES,ABI,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SSAHASNP,SSMP,TISHKOFF,20.542218
L2HGDHchr145072639050726391rs112494721+G-/Gdeletionintron21000GENOMES,BUSHMAN,20.447248
L2HGDHchr145072639250726393rs10132003+GA/Gsingleintron171000GENOMES,ABI,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.875856
L2HGDHchr145072650850726509rs145523936+GA/Gsingleintron11000GENOMES,20.011019
L2HGDHchr145072654750726548rs201522974+A-/Adeletionintron11000GENOMES,20.028007
L2HGDHchr145072672750726731rs201533838+AGAT-/AGATdeletionintron11000GENOMES,20.028467
L2HGDHchr145072697150726972rs75481167+CC/Tsingleintron71000GENOMES,BGI,BL,COMPLETE_GENOMICS,GMI,SSMP,TISHKOFF,20.778899
L2HGDHchr145072700950727010rs8013289+GC/Gsingleintron211000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.595479
L2HGDHchr145072710850727109rs8013174+CC/Gsingleintron211000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.419740
L2HGDHchr145072719350727194rs8013339+CA/Csingleintron191000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PJP,SSAHASNP,SSMP,WI_SSAHASNP,20.721099
L2HGDHchr145072721850727219rs11157732+AA/Tsingleintron171000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,20.461598
L2HGDHchr145072722750727228rs8013220+AA/Gsingleintron31000GENOMES,TISHKOFF,WI_SSAHASNP,20.948606
L2HGDHchr145072724250727243rs115765480+CA/Csingleintron21000GENOMES,TISHKOFF,20.014373
L2HGDHchr145072725150727252rs8013641+GA/Gsingleintron21000GENOMES,WI_SSAHASNP,20.010017
L2HGDHchr145072734850727349rs76507241+GA/Gsingleintron31000GENOMES,ILLUMINA,TISHKOFF,20.014808
L2HGDHchr145072748250727483rs10873033+GA/Gsingleintron171000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,20.500455
L2HGDHchr145072752250727523rs11157733+GA/Gsingleintron111000GENOMES,ABI,BGI,BL,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,ILLUMINA,SSMP,TISHKOFF,20.217749
L2HGDHchr145072860450728605rs76342915+AA/Tsingleintron21000GENOMES,TISHKOFF,20.962544
L2HGDHchr145072873550728736rs4901005+AA/Csingleintron201000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA-UK,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.411070
L2HGDHchr145072913250729133rs4901006+CC/Tsingleintron81000GENOMES,BL,COMPLETE_GENOMICS,GMI,HGSV,SSMP,TISHKOFF,WI_SSAHASNP,20.783883
L2HGDHchr145072924950729250rs4901007+AA/Gsingleintron191000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,KRIBB_YJKIM,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.522553
L2HGDHchr145072939750729398rs8004516+AA/Gsingleintron191000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,WUGSC_SSAHASNP,20.277842
L2HGDHchr145072942450729425rs8004684+CC/Tsingleintron51000GENOMES,ILLUMINA,KRIBB_YJKIM,TISHKOFF,WI_SSAHASNP,20.940113
L2HGDHchr145073007650730077rs10400736+TC/Tsingleintron61000GENOMES,BCM_SSAHASNP,BUSHMAN,COMPLETE_GENOMICS,ILLUMINA,SSMP,20.015373
L2HGDHchr145073018650730187rs75408779+AA/Gsingleintron21000GENOMES,ILLUMINA,20.989547
L2HGDHchr145073048350730484rs116713532+CA/Csingleintron11000GENOMES,20.010453
L2HGDHchr145073051450730515rs10400794+CC/Tsingleintron21000GENOMES,BCM_SSAHASNP,20.986685
L2HGDHchr145073066050730661rs10400739+TC/Tsingleintron71000GENOMES,ABI,BCM_SSAHASNP,BUSHMAN,COMPLETE_GENOMICS,SSMP,TISHKOFF,20.017415
L2HGDHchr145073081750730818rs35364406+CC/Tsingleintron61000GENOMES,ABI,BUSHMAN,COMPLETE_GENOMICS,SSMP,TISHKOFF,20.982585
L2HGDHchr145073083850730839rs112131693+TA/Tsingleintron31000GENOMES,COMPLETE_GENOMICS,SSMP,20.016514
L2HGDHchr145073115550731156rs115575336+CA/Csingleintron11000GENOMES,20.010453
L2HGDHchr145073135850731359rs34327481+AA/Gsingleintron71000GENOMES,ABI,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,SSMP,TISHKOFF,20.980347
L2HGDHchr145073149950731500rs112379465+GA/Gsingleintron21000GENOMES,COMPLETE_GENOMICS,20.011468
L2HGDHchr145073154750731549rs147763738+AT-/ATdeletionintron31000GENOMES,LUNTER,TISHKOFF,20.038108
L2HGDHchr145073159950731600rs8007752+TC/Tsingleintron21000GENOMES,WI_SSAHASNP,20.010453
L2HGDHchr145073162550731627rs148824535+AT-/ATdeletionintron21000GENOMES,LUNTER,20.034435
L2HGDHchr145073204150732042rs12432673+GA/Gsingleintron191000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,CLINSEQ_SNP,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,20.411286
L2HGDHchr145073262350732624rs114475843+CC/Tsingleintron11000GENOMES,20.989547
L2HGDHchr145073294650732947rs2355885+CC/Tsingleintron221000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.499305
L2HGDHchr145073323250733233rs61582827+TG/Tsingleintron61000GENOMES,BUSHMAN,COMPLETE_GENOMICS,HGSV,SSMP,TISHKOFF,20.012363
L2HGDHchr145073382450733825rs17715808+AA/Csingleintron51000GENOMES,COMPLETE_GENOMICS,ILLUMINA,PERLEGEN,SSMP,20.978898
L2HGDHchr145073388950733890rs143061401+TC/Tsingleintron11000GENOMES,20.020661
L2HGDHchr145073389350733894rs191191028+TC/Tsingleintron11000GENOMES,20.010101
L2HGDHchr145073390550733906rs181124381+TC/Tsingleintron11000GENOMES,20.073921
L2HGDHchr145073396250733963rs147064953+CC/Tsingleintron31000GENOMES,SSMP,TISHKOFF,20.922406
L2HGDHchr145073409950734100rs12431485+TC/Tsingleintron141000GENOMES,ABI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SSAHASNP,SSMP,TISHKOFF,20.543300
L2HGDHchr145073415150734152rs141957010+GA/Gsingleintron11000GENOMES,20.046832
L2HGDHchr145073418850734189rs112214370+TC/Tsingleintron41000GENOMES,BUSHMAN,COMPLETE_GENOMICS,SSMP,20.048055
L2HGDHchr145073427750734278rs12431539+TG/Tsingleintron91000GENOMES,ABI,BGI,BL,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,SSAHASNP,20.408425
L2HGDHchr145073428150734282rs12431540+TG/Tsingleintron141000GENOMES,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,20.706606
L2HGDHchr145073495650734957rs148656301+CC/Tsingleintron21000GENOMES,TISHKOFF,20.965565
L2HGDHchr145073532750735328rs74655060+GA/Gsingleintron11000GENOMES,20.013066
L2HGDHchr145073550450735505rs1040689+TC/Tsingleintron101000GENOMES,ABI,BUSHMAN,COMPLETE_GENOMICS,HGSV,ILLUMINA,PERLEGEN,SSMP,TISHKOFF,TSC-CSHL,20.047654
L2HGDHchr145073560150735602rs78813265+CC/Gsingleintron21000GENOMES,COMPLETE_GENOMICS,20.988532
L2HGDHchr145073561050735611rs17122336+GA/Gsingleintron51000GENOMES,HGSV,ILLUMINA,PERLEGEN,TISHKOFF,20.030635
L2HGDHchr145073564450735645rs60167764+AA/Csingleintron31000GENOMES,HGSV,TISHKOFF,20.962544
L2HGDHchr145073628650736287rs8015598+TC/Tsingleintron31000GENOMES,TISHKOFF,WI_SSAHASNP,20.010778
L2HGDHchr145073634150736342rs8015621+TA/Tsingleintron21000GENOMES,WI_SSAHASNP,20.010453
L2HGDHchr145073672450736725rs2153553+CC/Tsingleintron201000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.523644
L2HGDHchr145073731850737319rs4129162+GA/Gsingleintron71000GENOMES,ABI,COMPLETE_GENOMICS,SC_JCM,SSMP,TISHKOFF,TSC-CSHL,20.061927
L2HGDHchr145073766850737669rs4901008+AA/Gsingleintron191000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BGI,BL,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,KRIBB_YJKIM,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.590785
L2HGDHchr145073914150739142rs79971793+CC/Tsingleintron21000GENOMES,COMPLETE_GENOMICS,20.988532
L2HGDHchr145073948450739485rs11157734+AA/Csingleintron191000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PJP,SSAHASNP,SSMP,TISHKOFF,20.420120
L2HGDHchr145073994550739946rs147975298+A-/Adeletionintron21000GENOMES,LUNTER,20.011019
L2HGDHchr145074004650740047rs17406958+CC/Tsingleintron81000GENOMES,AFFY,BUSHMAN,COMPLETE_GENOMICS,ILLUMINA,KRIBB_YJKIM,PERLEGEN,SSMP,20.974159
L2HGDHchr145074019050740191rs2883802+AA/Csingleintron181000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.485858
L2HGDHchr145074027750740278rs114252236+TA/Tsingleintron11000GENOMES,20.039634
L2HGDHchr145074044950740450rs115185093+AA/Tsingleintron11000GENOMES,20.987805
L2HGDHchr145074060450740605rs11849020+CC/Tsingleintron161000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SSAHASNP,SSMP,TISHKOFF,20.424146
L2HGDHchr145074062750740628rs138491608+CC/Tsingleintron31000GENOMES,SSMP,TISHKOFF,20.929752
L2HGDHchr145074069950740700rs11849059+CA/Csingleintron141000GENOMES,BCM-HGSC-SUB,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SSAHASNP,SSMP,TISHKOFF,20.571885
L2HGDHchr145074103050741031rs35059048+AA/Gsingleintron31000GENOMES,ABI,ENSEMBL,20.989918
L2HGDHchr145074170650741707rs116748760+AA/Gsingleintron21000GENOMES,TISHKOFF,20.989111
L2HGDHchr145074189850741898rs142905920+--/Ainsertionintron41000GENOMES,LUNTER,SSMP,TISHKOFF,20.929752
L2HGDHchr145074224850742249rs4901009+TC/Tsingleintron231000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.738775
L2HGDHchr145074234050742341rs78262502+AA/Csingleintron41000GENOMES,COMPLETE_GENOMICS,ILLUMINA,TISHKOFF,20.962385
L2HGDHchr145074239150742392rs11851290+CC/Tsingleintron51000GENOMES,ABI,CSHL-HAPMAP,ENSEMBL,ILLUMINA,20.989214
L2HGDHchr145074254650742547rs57843266+TC/Tsingleintron61000GENOMES,BUSHMAN,COMPLETE_GENOMICS,HGSV,SSMP,TISHKOFF,20.047183
L2HGDHchr145074334350743344rs73275194+TC/Tsingleintron41000GENOMES,BUSHMAN,COMPLETE_GENOMICS,SSMP,20.012363
L2HGDHchr145074373150743732rs1465159+TC/Tsingleintron181000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.571922
L2HGDHchr145074446150744462rs140651628+GA/Gsingleintron11000GENOMES,20.011478
L2HGDHchr145074453750744538rs138479821+AA/Csingleintron11000GENOMES,20.968320
L2HGDHchr145074454050744541rs141380237+AA/Csingleintron11000GENOMES,20.975666
L2HGDHchr145074454350744544rs75718994+AA/Csingleintron41000GENOMES,BUSHMAN,ILLUMINA,ILLUMINA-UK,20.863365
L2HGDHchr145074522250745223rs73275195+CC/Tsingleintron41000GENOMES,BUSHMAN,COMPLETE_GENOMICS,NHLBI-ESP,20.989459
L2HGDHchr145074552450745525rs116571258+CC/Gsingleintron21000GENOMES,TISHKOFF,20.989111
L2HGDHchr145074579350745794rs114448496+TA/Tsingleintron11000GENOMES,20.010453
L2HGDHchr145074609650746097rs11332302+G-/Gdeletionintron91000GENOMES,ABI,BILGI_BIOE,DEVINE_LAB,GMI,LUNTER,PJP,SSMP,TISHKOFF,20.512397
L2HGDHchr145074617350746174rs74703322+AA/Gsingleintron31000GENOMES,BUSHMAN,TISHKOFF,20.964679
L2HGDHchr145074711150747112rs113479239+GC/Gsingleintron41000GENOMES,BUSHMAN,SSMP,TISHKOFF,20.013303
L2HGDHchr145074733650747337rs12432105+TG/Tsingleintron171000GENOMES,AFFY,BCM-HGSC-SUB,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA-UK,KRIBB_YJKIM,PJP,SSAHASNP,SSMP,TISHKOFF,20.555677
L2HGDHchr145074783050747831rs9743539+TG/Tsingleintron51000GENOMES,AFFY,BCM_SSAHASNP,ILLUMINA,KRIBB_YJKIM,20.011628
L2HGDHchr145074784950747850rs115253800+GC/Gsingleintron11000GENOMES,20.010889
L2HGDHchr145074812550748126rs7149462+CA/C/Gsingleintron31000GENOMES,BCM_SSAHASNP,TISHKOFF,20.965565
L2HGDHchr145074842250748423rs192703645+GA/Gsingleintron11000GENOMES,20.033517
L2HGDHchr145074842750748427rs200178997+--/Ginsertionintron11000GENOMES,20.966024
L2HGDHchr145074885250748853rs12889265+TC/Tsingleintron161000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,20.566485
L2HGDHchr145074986650749867rs151333705+CC/Tsingleintron21000GENOMES,SSMP,20.989899
L2HGDHchr145074992050749921rs113149074+G-/Gdeletionintron31000GENOMES,BUSHMAN,LUNTER,20.357798
L2HGDHchr145074992350749924rs8019274+GA/Gsingleintron121000GENOMES,BCM-HGSC-SUB,BGI,BL,COMPLETE_GENOMICS,ENSEMBL,GMI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,WI_SSAHASNP,20.439662
L2HGDHchr145075031550750316rs12432978+CC/Tsingleintron171000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,20.440230
L2HGDHchr145075057650750577rs12433038+AA/Gsingleintron221000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,20.492315
L2HGDHchr145075077850750779rs10135842+GA/Gsingleintron121000GENOMES,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,SSMP,TISHKOFF,WI_SSAHASNP,20.143935
L2HGDHchr145075118250751183rs10483597-GA/Csingleintron101000GENOMES,AFFY,BCMHGSC_JDW,ENSEMBL,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,SSMP,TISHKOFF,20.038511
L2HGDHchr145075119950751199rs11460377+--/Tinsertionintron101000GENOMES,ABI,BILGI_BIOE,DEVINE_LAB,GMI,HUMANGENOME_JCVI,LUNTER,PJP,SSMP,TISHKOFF,20.494495
L2HGDHchr145075156450751565rs6572655+GG/Tsingleintron221000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.410453
L2HGDHchr145075169150751692rs142815942+GA/Gsingleintron21000GENOMES,ILLUMINA,20.018366
L2HGDHchr145075221950752220rs8004572+CC/Tsingleintron201000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.078986
L2HGDHchr145075258350752584rs78761462+TC/Tsingleintron31000GENOMES,ILLUMINA,TISHKOFF,20.040070
L2HGDHchr145075275750752758rs75473886+TC/Tsingleintron21000GENOMES,TISHKOFF,20.010889
L2HGDHchr145075287550752876rs12882001+TC/Tsingleintron101000GENOMES,ABI,AFFY,ENSEMBL,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,PERLEGEN,PJP,SSAHASNP,20.036612
L2HGDHchr145075307350753073rs149572581+--/Ainsertionintron21000GENOMES,LUNTER,20.979798
L2HGDHchr145075324150753242rs11849603+CC/Gsingleintron191000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,20.422561
L2HGDHchr145075356250753563rs17122352+CC/Tsingleintron31000GENOMES,PERLEGEN,TISHKOFF,20.965693
L2HGDHchr145075370650753707rs116475753+TC/Tsingleintron11000GENOMES,20.010889
L2HGDHchr145075381750753818rs115313890+CA/Csingleintron21000GENOMES,TISHKOFF,20.020035
L2HGDHchr145075382650753827rs12886516+GG/Tsingleintron111000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PERLEGEN,PJP,SSAHASNP,SSMP,30.821075
L2HGDHchr145075399150753992rs7154966+TC/Tsingleintron181000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,20.583485
L2HGDHchr145075424950754250rs80027895+TC/Tsingleintron11000GENOMES,20.038328
L2HGDHchr145075468050754681rs12436483+AA/Gsingleintron121000GENOMES,ABI,BCMHGSC_JDW,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,PJP,SSAHASNP,SSMP,TISHKOFF,20.494521
L2HGDHchr145075470950754710rs12436501+CC/Tsingleintron141000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SSAHASNP,SSMP,TISHKOFF,20.599087
L2HGDHchr145075496850754969rs17716174+AA/Csingleintron91000GENOMES,AFFY,BCMHGSC_JDW,ENSEMBL,ILLUMINA,ILLUMINA-UK,PERLEGEN,SSMP,TISHKOFF,20.941567
L2HGDHchr145075508750755088rs78712705+CC/Tsingleintron11000GENOMES,20.986934
L2HGDHchr145075536150755362rs113177564+CC/Tsingleintron41000GENOMES,COMPLETE_GENOMICS,SSMP,TISHKOFF,20.867431
L2HGDHchr145075537350755374rs138038370+CC/Tsingleintron11000GENOMES,20.985308
L2HGDHchr145075538550755386rs74889514+TC/Tsingleintron41000GENOMES,ILLUMINA-UK,SSMP,TISHKOFF,20.070642
L2HGDHchr145075567050755671rs8022617+CC/Tsingleintron171000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.472668
L2HGDHchr145075585650755857rs111937527+AA/Gsingleintron41000GENOMES,BUSHMAN,COMPLETE_GENOMICS,TISHKOFF,20.988084
L2HGDHchr145075599050755991rs12881896+CC/Tsingleintron151000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PERLEGEN,PJP,SSAHASNP,SSMP,20.420985
L2HGDHchr145075601950756020rs74735522+TC/Tsingleintron21000GENOMES,ILLUMINA,20.015679
L2HGDHchr145075608850756089rs12882050+CC/Tsingleintron141000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,20.431189
L2HGDHchr145075638450756385rs17122355+TC/Tsingleintron51000GENOMES,BUSHMAN,COMPLETE_GENOMICS,PERLEGEN,SSMP,20.012048
L2HGDHchr145075639550756396rs17778466+AA/Tsingleintron51000GENOMES,BCMHGSC_JDW,ENSEMBL,PERLEGEN,SSMP,20.948251
L2HGDHchr145075671150756712rs139363658+AA/Gsingleintron21000GENOMES,TISHKOFF,20.965565
L2HGDHchr145075680950756810rs181098653+TC/Tsingleintron21000GENOMES,TISHKOFF,20.034435
L2HGDHchr145075698650756986rs199797742+--/Ainsertionintron11000GENOMES,20.971074
L2HGDHchr145075709450757095rs9888568+CC/Tsingleintron181000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,20.489091
L2HGDHchr145075713050757131rs9888567+AA/Csingleintron181000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA-UK,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,20.412644
L2HGDHchr145075759450757594rs199628176+--/Tinsertionintron21000GENOMES,LUNTER,20.988062
L2HGDHchr145075784750757848rs112703335+GA/Gsingleintron51000GENOMES,BUSHMAN,COMPLETE_GENOMICS,SSMP,TISHKOFF,20.022904
L2HGDHchr145075821850758219rs116330607+AA/Gsingleintron11000GENOMES,20.989111
L2HGDHchr145075825250758253rs17122357+GA/Gsingleintron61000GENOMES,AFFY,ILLUMINA,KRIBB_YJKIM,PERLEGEN,TISHKOFF,20.038080
L2HGDHchr145075856450758565rs7158883+TC/Tsingleintron91000GENOMES,BCM_SSAHASNP,BUSHMAN,COMPLETE_GENOMICS,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,SSMP,TISHKOFF,20.153706
L2HGDHchr145075881650758821rs149022072+AATAT-/AATATdeletionintron31000GENOMES,LUNTER,SSMP,20.070248
L2HGDHchr145075920250759203rs12586416+TC/Tsingleintron131000GENOMES,ABI,BCM-HGSC-SUB,BGI,BL,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,PJP,SSAHASNP,SSMP,TISHKOFF,20.410959
L2HGDHchr145075926050759261rs7141428+CC/Tsingleintron31000GENOMES,BCM_SSAHASNP,TISHKOFF,20.989111
L2HGDHchr145075935250759353rs61242556+GA/Gsingleintron61000GENOMES,BUSHMAN,COMPLETE_GENOMICS,HGSV,SSMP,TISHKOFF,20.046309
L2HGDHchr145075946250759463rs60116101+TC/Tsingleintron61000GENOMES,BUSHMAN,COMPLETE_GENOMICS,HGSV,SSMP,TISHKOFF,20.045392
L2HGDHchr145075967750759678rs7142135+AA/Gsingleintron181000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,20.423760
L2HGDHchr145075986650759867rs114515014+TC/Tsingleintron21000GENOMES,TISHKOFF,20.041376
L2HGDHchr145076002850760029rs116103825+CA/Csingleintron21000GENOMES,TISHKOFF,20.010889
L2HGDHchr145076002950760030rs12894758+CC/Tsingleintron141000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,COMPLETE_GENOMICS,ENSEMBL,GMI,ILLUMINA,KRIBB_YJKIM,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,20.822979
L2HGDHchr145076025050760251rs11851584+AA/Tsingleintron101000GENOMES,ABI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,ILLUMINA-UK,PERLEGEN,SSMP,TISHKOFF,20.863832
L2HGDHchr145076038150760382rs76346958+CA/Csingleintron21000GENOMES,TISHKOFF,20.037456
L2HGDHchr145076038350760384rs56747827+GA/Gsingleintron61000GENOMES,BUSHMAN,COMPLETE_GENOMICS,HGSV,SSMP,TISHKOFF,20.011905
L2HGDHchr145076046550760466rs56820086+TC/Tsingleintron61000GENOMES,BUSHMAN,COMPLETE_GENOMICS,HGSV,SSMP,TISHKOFF,20.011905
L2HGDHchr145076184650761847rs7144289+GC/Gsingleintron181000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,20.541971
L2HGDHchr145076227050762271rs117382920+TC/Tsingleintron21000GENOMES,SSMP,20.017406
L2HGDHchr145076270050762701rs7151147+TC/Tsingleintron91000GENOMES,BCM_SSAHASNP,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,SSMP,20.708467
L2HGDHchr145076410750764107rs148803952+--/Ainsertionintron31000GENOMES,LUNTER,TISHKOFF,20.968779
L2HGDHchr145076509650765097rs190103238+GC/Gsingleintron31000GENOMES,GMI,SSMP,20.016529
L2HGDHchr145076521050765211rs113231941+TG/Tsingleintron51000GENOMES,BUSHMAN,COMPLETE_GENOMICS,SSMP,TISHKOFF,20.047204
L2HGDHchr145076575750765758rs4901010+GA/Gsingleintron151000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,GMI,HUMANGENOME_JCVI,ILLUMINA-UK,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.506014
L2HGDHchr145076592350765924rs80190354+AA/Gsingleintron41000GENOMES,ILLUMINA-UK,SSMP,TISHKOFF,20.927982
L2HGDHchr145076602850766029rs2153554+AA/Gsingleintron101000GENOMES,ABI,BUSHMAN,ILLUMINA-UK,PERLEGEN,SC_JCM,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.864265
L2HGDHchr145076750450767505rs113989112+CC/Tsingleintron,near-gene-541000GENOMES,BUSHMAN,COMPLETE_GENOMICS,SSMP,20.988084
L2HGDHchr145076754850767549rs116110419+TC/Tsingleintron,near-gene-511000GENOMES,20.011760
L2HGDHchr145076775150767752rs111526615+CC/Tsingleintron,near-gene-541000GENOMES,BUSHMAN,COMPLETE_GENOMICS,SSMP,20.987637
L2HGDHchr145076781350767814rs73277317+CC/Gsingleintron,near-gene-541000GENOMES,BUSHMAN,COMPLETE_GENOMICS,SSMP,20.987637
L2HGDHchr145076787350767874rs112771654+GA/Gsingleintron,near-gene-541000GENOMES,BUSHMAN,COMPLETE_GENOMICS,SSMP,20.012374
L2HGDHchr145076838950768390rs61584633+AA/Gsingleintron,near-gene-561000GENOMES,BUSHMAN,COMPLETE_GENOMICS,HGSV,SSMP,TISHKOFF,20.980311
L2HGDHchr145076848250768483rs4901011+AA/Gsingleintron,near-gene-5181000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.423304
L2HGDHchr145076858750768588rs73277322+CC/Tsingleintron,near-gene-531000GENOMES,BUSHMAN,COMPLETE_GENOMICS,20.989464
L2HGDHchr145076869850768699rs41299197+TC/Tsingleintron61000GENOMES,CLINSEQ_SNP,HGSV,ILLUMINA,NHLBI-ESP,SI_EXO,20.043349
L2HGDHchr145076932650769327rs2297993+AA/Gsingleintron211000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,YUSUKE,20.415183
L2HGDHchr145076935550769356rs115316721+CC/Tsingleintron21000GENOMES,TISHKOFF,20.989111
L2HGDHchr145076938450769385rs55851766+CC/Tsingleintron61000GENOMES,BUSHMAN,HGSV,ILLUMINA-UK,SSMP,TISHKOFF,20.924840
L2HGDHchr145076945450769455rs2297994+GG/Tsingleintron181000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,YUSUKE,20.428298
L2HGDHchr145076985850769859rs17122363+CC/Tsingleintron51000GENOMES,BUSHMAN,COMPLETE_GENOMICS,PERLEGEN,SSMP,20.987511
L2HGDHchr145076986750769868rs1962578+GA/Gsingleintron141000GENOMES,ABI,BL,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.415525
L2HGDHchr145076990050769901rs1974327+AA/Gsingleintron161000GENOMES,ABI,BCMHGSC_JDW,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.428377
L2HGDHchr145077001450770015rs1962579+CA/C/G/Tsingleintron171000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.479252
L2HGDHchr145077004250770043rs112503230+GA/Gsingleintron21000GENOMES,COMPLETE_GENOMICS,20.021101
L2HGDHchr145077052050770521rs1557010+GG/Tsingleintron131000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,SC_JCM,SSAHASNP,SSMP,TSC-CSHL,20.100000
L2HGDHchr145077098450770985rs79207710+GA/Gsingleintron21000GENOMES,TISHKOFF,20.039634
L2HGDHchr145077240250772403rs8018446+CC/Tsingleintron181000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.427335
L2HGDHchr145077273350772734rs11851370+CC/Tsingleintron181000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,20.464286
L2HGDHchr145077279950772800rs192789987+GG/Tsingleintron11000GENOMES,20.969697
L2HGDHchr145077307450773075rs73277332+TG/Tsingleintron51000GENOMES,BUSHMAN,COMPLETE_GENOMICS,SSMP,TISHKOFF,20.011916
L2HGDHchr145077328850773289rs113886089+T-/Tdeletionintron21000GENOMES,BUSHMAN,20.118349
L2HGDHchr145077329550773296rs946993+TG/Tsingleintron171000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TSC-CSHL,WI_SSAHASNP,20.494632
L2HGDHchr145077330950773310rs200320716+G-/Gdeletionintron11000GENOMES,20.069789
L2HGDHchr145077342650773427rs17122365+TC/Tsingleintron41000GENOMES,ILLUMINA,ILLUMINA-UK,PERLEGEN,20.011628
L2HGDHchr145077353850773539rs78230395+TA/Tsingleintron31000GENOMES,BL,GMI,20.209385
L2HGDHchr145077353950773540rs12880166+TA/Tsingleintron141000GENOMES,ABI,BCMHGSC_JDW,BGI,BL,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,20.553522
L2HGDHchr145077357550773576rs12880323+TC/Tsingleintron171000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,20.572599
L2HGDHchr145077386950773870rs7143204+TG/Tsingleintron91000GENOMES,BCM_SSAHASNP,BGI,BL,GMI,ILLUMINA,PJP,SSMP,WI_SSAHASNP,20.197075
L2HGDHchr145077450350774504rs73277336+GC/Gsingleintron41000GENOMES,BUSHMAN,COMPLETE_GENOMICS,SSMP,20.012363
L2HGDHchr145077483050774831rs73277339+GA/Gsingleintron51000GENOMES,BUSHMAN,COMPLETE_GENOMICS,ILLUMINA,TISHKOFF,20.012363
L2HGDHchr145077505350775054rs8015010+GA/Gsingleintron41000GENOMES,COMPLETE_GENOMICS,ILLUMINA-UK,WI_SSAHASNP,20.021540
L2HGDHchr145077531850775319rs6572656+CA/Csingleintron181000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSMP,TISHKOFF,WI_SSAHASNP,20.579732
L2HGDHchr145077547550775476rs12433317+GA/Gsingleintron131000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SSMP,TISHKOFF,20.428245
L2HGDHchr145077574050775750rs144747446+TTTTGAGAGT-/TTTTGAGAGTdeletionintron41000GENOMES,BILGI_BIOE,GMI,LUNTER,20.521579
L2HGDHchr145077600550776006rs112733256+TG/Tsingleintron41000GENOMES,COMPLETE_GENOMICS,SSMP,TISHKOFF,20.038073
L2HGDHchr145077624050776241rs7158964+CC/Tsingleintron121000GENOMES,BCMHGSC_JDW,BCM_SSAHASNP,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SSMP,TISHKOFF,20.409859
L2HGDHchr145077629750776298rs114696998+AA/Csingleintron11000GENOMES,20.986934
L2HGDHchr145077653250776533rs112083596+TA/Tsingleintron21000GENOMES,COMPLETE_GENOMICS,20.011009
L2HGDHchr145077654450776545rs8021001+AA/Gsingleintron161000GENOMES,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.423883
L2HGDHchr145077658650776587rs116023915+TC/Tsingleintron21000GENOMES,TISHKOFF,20.011760
L2HGDHchr145077686350776864rs77039032+TA/Tsingleintron21000GENOMES,TISHKOFF,20.021777
L2HGDHchr145077689650776897rs79988677+TG/Tsingleintron21000GENOMES,TISHKOFF,20.022213
L2HGDHchr145077742950777430rs8007800+TC/Tsingleintron,near-gene-5141000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSMP,WI_SSAHASNP,20.545247
L2HGDHchr145077765850777659rs188617542+TC/Tsingleintron,near-gene-511000GENOMES,20.100092
L2HGDHchr145077765850777658rs200515426+--/Cinsertionintron,near-gene-511000GENOMES,20.899449
L2HGDHchr145077826850778268rs72473098+--/Tinsertionintron,near-gene-551000GENOMES,DEVINE_LAB,LUNTER,SSMP,TISHKOFF,20.872819
DUOX2chr154538665545386656rs7171366+TG/Tsingleintron141000GENOMES,BCM_SSAHASNP,BL,BUSHMAN,COMPLETE_GENOMICS,GMI,HGSV,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SSMP,TISHKOFF,20.231763
DUOX2chr154538738845387389rs111280439+AA/Csingleintron31000GENOMES,BUSHMAN,TISHKOFF,20.984418
DUOX2chr154538754945387550rs199138-AC/Tsingleintron201000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,KWOK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.703597
DUOX2chr154538789845387899rs16977579+TC/Tsingleintron91000GENOMES,AFFY,BUSHMAN,COMPLETE_GENOMICS,HGSV,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,TISHKOFF,20.116008
DUOX2chr154538838145388382rs2554451-CA/Gsingleintron171000GENOMES,ABI,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.738897
DUOX2chr154538839445388395rs73406323+GA/Gsingleintron51000GENOMES,BUSHMAN,COMPLETE_GENOMICS,ILLUMINA-UK,TISHKOFF,20.076853
DUOX2chr154538872645388727rs73406325+AA/Tsingleintron61000GENOMES,BUSHMAN,COMPLETE_GENOMICS,ILLUMINA-UK,SSMP,TISHKOFF,20.884369
DUOX2chr154539094545390946rs111702374+GA/Gsingleintron31000GENOMES,BUSHMAN,TISHKOFF,20.015582
DUOX2chr154539121045391211rs146865634+C-/Cdeletionintron11000GENOMES,20.039027
DUOX2chr154539129345391294rs4774515+CC/Tsingleintron41000GENOMES,SSMP,TISHKOFF,WI_SSAHASNP,20.960587
DUOX2chr154539145445391455rs56833067+AA/Gsingleintron71000GENOMES,BUSHMAN,COMPLETE_GENOMICS,GMI,HGSV,SSMP,TISHKOFF,20.800824
DUOX2chr154539149845391499rs113618416+CC/Tsingleintron41000GENOMES,BUSHMAN,SSMP,TISHKOFF,20.961962
DUOX2chr154539152445391525rs111613241+AA/Gsingleintron31000GENOMES,BUSHMAN,TISHKOFF,20.984418
DUOX2chr154539215445392155rs143612396+CC/Gsingleintron21000GENOMES,TISHKOFF,20.987603
DUOX2chr154539251645392517rs77512689+CA/Csingleintron21000GENOMES,TISHKOFF,20.031794
DUOX2chr154539277745392778rs79374174+GC/Gsingleintron31000GENOMES,BUSHMAN,TISHKOFF,20.014679
DUOX2chr154539281145392812rs76356689+GA/Gsingleintron41000GENOMES,BUSHMAN,SSMP,TISHKOFF,20.037580
DUOX2chr154539290045392901rs75048501+CC/Tsingleintron51000GENOMES,BUSHMAN,ILLUMINA,NHLBI-ESP,TISHKOFF,20.984876
DUOX2chr154539336045393361rs111706445+GA/Gsingleintron31000GENOMES,BUSHMAN,NHLBI-ESP,20.010092
DUOX2chr154539366645393667rs953733+AA/Gsingleintron111000GENOMES,BL,BUSHMAN,COMPLETE_GENOMICS,GMI,ILLUMINA,ILLUMINA-UK,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.848717
DUOX2chr154539392945393930rs78256554+GA/Gsingleintron41000GENOMES,BUSHMAN,SSMP,TISHKOFF,20.037580
DUOX2chr154539440545394406rs269866-GC/Tsingleintron221000GENOMES,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,KWOK,PERLEGEN,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.466145
DUOX2chr154539451845394519rs116562151+CA/Csingleintron21000GENOMES,TISHKOFF,20.016551
DUOX2chr154539458245394583rs111477569+GA/Gsingleintron31000GENOMES,COMPLETE_GENOMICS,TISHKOFF,20.031193
DUOX2chr154539481145394812rs112473943+GA/Gsingleintron41000GENOMES,BUSHMAN,ILLUMINA,TISHKOFF,20.015124
DUOX2chr154539492045394921rs56838826+TC/Tsingleintron91000GENOMES,BL,BUSHMAN,COMPLETE_GENOMICS,GMI,HGSV,ILLUMINA-UK,SSMP,TISHKOFF,20.091491
DUOX2chr154539558345395584rs61626661+AA/Gsingleintron91000GENOMES,BL,BUSHMAN,COMPLETE_GENOMICS,GMI,HGSV,ILLUMINA-UK,SSMP,TISHKOFF,20.924943
DUOX2chr154539564445395644rs143847058+--/Tinsertionintron21000GENOMES,BL,20.980257
DUOX2chr154539579545395796rs112432895+AA/Gsingleintron31000GENOMES,BUSHMAN,TISHKOFF,20.984418
DUOX2chr154539628845396289rs113684942+TC/Tsingleintron51000GENOMES,BUSHMAN,ILLUMINA,NHLBI-ESP,TISHKOFF,20.016972
DUOX2chr154539661145396612rs80095330+TC/Tsingleintron41000GENOMES,ILLUMINA,NHLBI-ESP,TISHKOFF,20.030488
DUOX2chr154539674945396750rs113078084+AA/Gsingleintron31000GENOMES,BUSHMAN,TISHKOFF,20.984418
DUOX2chr154539720245397203rs141433708+GA/G/Tsingleintron21000GENOMES,TISHKOFF,20.028007
DUOX2chr154539756545397566rs269863-GC/Gsingleintron181000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,KWOK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.265925
DUOX2chr154539783045397831rs73406330+GA/Gsingleintron111000GENOMES,BL,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,GMI,ILLUMINA,ILLUMINA-UK,NHLBI-ESP,SSMP,TISHKOFF,20.120867
DUOX2chr154539808845398089rs79849154+CC/Gsingleintron21000GENOMES,TISHKOFF,20.982143
DUOX2chr154539812645398127rs115012702+CC/Tsingleintron11000GENOMES,20.988676
DUOX2chr154539823045398231rs73406335+TG/Tsingleintron81000GENOMES,BL,BUSHMAN,COMPLETE_GENOMICS,GMI,ILLUMINA-UK,SSMP,TISHKOFF,20.123400
DUOX2chr154539831345398314rs73406337+GA/Gsingleintron111000GENOMES,BL,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,GMI,ILLUMINA,ILLUMINA-UK,NHLBI-ESP,SSMP,TISHKOFF,20.071040
DUOX2chr154539862845398629rs79757509+TC/Tsingleintron21000GENOMES,SSMP,20.024390
DUOX2chr154539896445398965rs269862-GA/Csingleintron221000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,KWOK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.825515
DUOX2chr154539931045399311rs78922026+CC/Tsingleintron31000GENOMES,ILLUMINA,SSMP,20.975610
DUOX2chr154539946645399467rs190599-AC/Tsingleintron211000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,KWOK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,YUSUKE,20.865771
DUOX2chr154539953245399533rs76411432+CC/Tsingleintron41000GENOMES,ILLUMINA,NHLBI-ESP,SSMP,20.975610
DUOX2chr154539999145399992rs166574-TA/Gsingleintron181000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,KWOK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.252737
DUOX2chr154540001345400014rs142530819+AA/Csingleintron21000GENOMES,SSMP,20.986226
DUOX2chr154540012145400122rs116831463+GA/Gsingleintron21000GENOMES,SSMP,20.023955
DUOX2chr154540016345400164rs269861-TA/Gsingleintron181000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,KWOK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.164695
DUOX2chr154540044845400449rs117599686+GA/Gsingleintron51000GENOMES,CLINSEQ_SNP,ILLUMINA,NHLBI-ESP,SSMP,20.011127
DUOX2chr154540044945400450rs79570265+CC/Tsingleintron31000GENOMES,NHLBI-ESP,SSMP,20.975610
DUOX2chr154540061145400611rs200873281+--/Ginsertionintron11000GENOMES,20.910468
DUOX2chr154540061345400613rs144393243+--/Cinsertionintron41000GENOMES,GMI,LUNTER,SSMP,20.921947
DUOX2chr154540163545401636rs1961660+CC/Tsingleintron141000GENOMES,ABI,BL,BUSHMAN,COMPLETE_GENOMICS,GMI,HGSV,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,SC_JCM,SSMP,TISHKOFF,TSC-CSHL,20.808531
DUOX2chr154540231845402319rs111737855+TC/Tsingleintron71000GENOMES,BL,BUSHMAN,GMI,ILLUMINA,SSMP,TISHKOFF,20.072377
DUOX2chr154540242845402429rs72724247+TG/Tsingleintron31000GENOMES,GMI,ILLUMINA,20.011019
DUOX2chr154540247845402479rs113324656+AA/Gsingleintron31000GENOMES,BUSHMAN,TISHKOFF,20.985321
DUOX2chr154540293945402940rs269859-AC/Tsingleintron211000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,KWOK,NHLBI-ESP,PJP,SC_JCM,SC_SNP,SSAHASNP,SSMP,TISHKOFF,20.814868
DUOX2chr154540296445402965rs114240217+GG/Tsingleintron31000GENOMES,NHLBI-ESP,TISHKOFF,20.969948
DUOX2chr154540298945402990rs80231352+GC/Gsingleintron31000GENOMES,GMI,SSMP,20.012620
DUOX2chr154540301645403017rs74011359+AA/Gsingleintron31000GENOMES,ILLUMINA-UK,SSMP,20.985780
DUOX2chr154540303645403037rs113800136+GA/Gsingleintron41000GENOMES,COMPLETE_GENOMICS,SSMP,TISHKOFF,20.011468
DUOX2chr154540309545403096rs2412956+TG/Tsingleintron151000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.983516
DUOX2chr154540351145403512rs200998617+CA/Csingleintron11000GENOMES,20.045454
DUOX2chr154540391645403917rs181503132+CC/Tsingleintron21000GENOMES,TISHKOFF,20.984848
DUOX2chr154540469245404693rs751151-CA/Gsingleintron,near-gene-581000GENOMES,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,ILLUMINA,SSMP,TISHKOFF,TSC-CSHL,20.051817
DUOX2chr154540469845404699rs76180151+CC/Tsingleintron,near-gene-571000GENOMES,BL,CLINSEQ_SNP,GMI,ILLUMINA,SSMP,TISHKOFF,20.968483
DUOX2chr154540499645404997rs113700172+CC/Tsingleintron,near-gene-531000GENOMES,BUSHMAN,TISHKOFF,20.985321
DUOX2chr154540514545405146rs74367551+GG/Tsingleintron,near-gene-551000GENOMES,BUSHMAN,ILLUMINA,NHLBI-ESP,TISHKOFF,20.971127
DUOX2chr154540532245405323rs77078382+CA/Csingleintron,near-gene-531000GENOMES,NHLBI-ESP,TISHKOFF,20.029617
DUOX2chr154540541345405414rs75354193+CC/Tsingleintron,near-gene-521000GENOMES,TISHKOFF,20.969948
DUOX2chr154540546245405463rs269856+GG/Tsingleintron,near-gene-5221000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,KWOK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.141864
DUOX2chr154540598645405987rs269855-GC/Tsingleintron,near-gene-5221000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,KWOK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.038063
ETFAchr157651003576510036rs116724809+CA/Csingleintron11000GENOMES,20.012631
ETFAchr157651007276510073rs1533600-GC/Tsingleintron231000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.029300
ETFAchr157651024076510241rs79195417+GA/Gsingleintron21000GENOMES,ILLUMINA,20.012631
ETFAchr157651030376510304rs12916022+GA/Gsingleintron131000GENOMES,ABI,BCM-HGSC-SUB,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SSAHASNP,SSMP,TISHKOFF,20.391781
ETFAchr157651052476510525rs114145226+GA/Gsingleintron21000GENOMES,TISHKOFF,20.026568
ETFAchr157651058176510582rs2245180-GC/Tsingleintron241000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.027350
ETFAchr157651069576510696rs2469570+TC/Tsingleintron181000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.964025
ETFAchr157651069976510700rs62030229+CC/Tsingleintron61000GENOMES,BCMHGSC_JDW,ENSEMBL,GMI,SSMP,TISHKOFF,20.748168
ETFAchr157651140476511405rs80154152+AA/Gsingleintron21000GENOMES,TISHKOFF,20.972561
ETFAchr157651198076511981rs79641522+GA/Gsingleintron21000GENOMES,TISHKOFF,20.027439
ETFAchr157651202676512027rs2456039-AC/Tsingleintron191000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.978578
ETFAchr157651235676512357rs72736862+AA/Gsingleintron31000GENOMES,SSMP,TISHKOFF,20.942467
ETFAchr157651240676512407rs11853864+CC/Tsingleintron41000GENOMES,BUSHMAN,CSHL-HAPMAP,ENSEMBL,20.983516
ETFAchr157651297576512976rs117827176+CC/Tsingleintron21000GENOMES,ILLUMINA,20.986510
ETFAchr157651299976513000rs117973661+TG/Tsingleintron41000GENOMES,GMI,ILLUMINA,SSMP,20.023499
ETFAchr157651323976513240rs34213321+AA/Gsingleintron131000GENOMES,ABI,BCM-HGSC-SUB,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SSMP,TISHKOFF,20.591241
ETFAchr157651355276513553rs2469571+GA/Gsingleintron211000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,KRIBB_YJKIM,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.924125
ETFAchr157651362676513627rs62030230+AA/Csingleintron71000GENOMES,BCMHGSC_JDW,BL,ENSEMBL,GMI,SSMP,TISHKOFF,20.936239
ETFAchr157651396576513966rs76634793+AA/Tsingleintron11000GENOMES,20.973868
ETFAchr157651436076514361rs11072578+AA/Gsingleintron141000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PERLEGEN,PJP,SSMP,20.670815
ETFAchr157651458976514591rs199626564+AA-/AAdeletionintron11000GENOMES,20.016070
ETFAchr157651466776514668rs11475733+T-/Tdeletionintron71000GENOMES,BILGI_BIOE,DEVINE_LAB,GMI,LUNTER,PJP,SSMP,20.350781
ETFAchr157651489576514896rs77815174+TC/Tsingleintron31000GENOMES,GMI,SSMP,20.051282
ETFAchr157651494476514945rs55772702+CC/Tsingleintron61000GENOMES,BL,BUSHMAN,HGSV,ILLUMINA,SSMP,20.926147
ETFAchr157651503176515031rs147485608+--/Ainsertionintron31000GENOMES,LUNTER,TISHKOFF,20.973829
ETFAchr157651511976515120rs883993+GC/Gsingleintron101000GENOMES,AFFY,BCM-HGSC-SUB,BGI,GMI,ILLUMINA-UK,KRIBB_YJKIM,SSMP,TISHKOFF,TSC-CSHL,20.353994
ETFAchr157651528076515281rs1810347-AG/Tsingleintron211000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.943431
ETFAchr157651570376515704rs7175022+AA/Gsingleintron71000GENOMES,BCMHGSC_JDW,BCM_SSAHASNP,BL,ENSEMBL,SSMP,TISHKOFF,20.941797
ETFAchr157651704776517048rs3784449+GA/Gsingleintron161000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,COMPLETE_GENOMICS,ENSEMBL,GMI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SSMP,TISHKOFF,YUSUKE,20.354613
ETFAchr157651716676517167rs2456038-AC/Tsingleintron201000GENOMES,ABI,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.946574
ETFAchr157651787676517877rs56233972+GA/G/Tsingleintron71000GENOMES,BCMHGSC_JDW,BL,ENSEMBL,HGSV,SSMP,TISHKOFF,20.060092
ETFAchr157651789376517894rs145400891+TC/Tsingleintron21000GENOMES,SSMP,20.051423
ETFAchr157651834576518345rs200152795+--/Cinsertionintron11000GENOMES,20.049587
ETFAchr157651863976518640rs62030232+TG/Tsingleintron91000GENOMES,BCMHGSC_JDW,BGI,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,ILLUMINA-UK,SSMP,20.351487
ETFAchr157651894076518941rs148568611+CC/Tsingleintron11000GENOMES,20.984389
ETFAchr157651894876518949rs141994554+GA/Gsingleintron11000GENOMES,20.010101
ETFAchr157651907576519076rs150704896+CC/Tsingleintron11000GENOMES,20.987603
ETFAchr157651913376519134rs11631764+GA/Gsingleintron91000GENOMES,ABI,BCMHGSC_JDW,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,SSAHASNP,SSMP,20.320642
ETFAchr157651913576519136rs11631690+CC/Tsingleintron91000GENOMES,ABI,BCMHGSC_JDW,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,SSAHASNP,SSMP,20.684404
ETFAchr157651920576519206rs2957036+TC/Tsingleintron151000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BL,BUSHMAN,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SC_JCM,SSAHASNP,SSMP,20.962997
ETFAchr157651948076519481rs75375526+AA/Gsingleintron31000GENOMES,BCM-HGSC-SUB,GMI,20.984769
ETFAchr157651955976519560rs144051186+GA/Gsingleintron21000GENOMES,SSMP,20.014692
ETFAchr157652036376520364rs78057253+TG/Tsingleintron21000GENOMES,TISHKOFF,20.039199
ETFAchr157652067576520676rs1518964-CA/Gsingleintron51000GENOMES,ABI,BUSHMAN,TISHKOFF,TSC-CSHL,20.015396
ETFAchr157652084176520842rs74762436+AA/Csingleintron21000GENOMES,BUSHMAN,20.984404
ETFAchr157652176976521770rs3898352-GC/Tsingleintron181000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,CSHL-HAPMAP,ENSEMBL,GMI,ILLUMINA,ILLUMINA-UK,PERLEGEN,PJP,SC_JCM,SC_SNP,SSMP,TISHKOFF,TSC-CSHL,20.663866
ETFAchr157652179776521798rs959991+CC/Tsingleintron181000GENOMES,ABI,BCM-HGSC-SUB,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,PJP,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.638609
ETFAchr157652203976522040rs1047357-GC/Tsingleintron41000GENOMES,AFFY,LEE,TISHKOFF,20.967432
ETFAchr157652210376522104rs4886783+AA/Gsingleintron161000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PJP,SSMP,TISHKOFF,WI_SSAHASNP,20.699279
ETFAchr157652220576522206rs78528554+TC/Tsingleintron11000GENOMES,20.011760
ETFAchr157652285676522857rs186147590+TG/Tsingleintron11000GENOMES,20.200643
ETFAchr157652294176522942rs2405326-TA/Gsingleintron141000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,SSAHASNP,SSMP,TSC-CSHL,20.051645
ETFAchr157652298176522982rs7175442+GG/Tsingleintron31000GENOMES,BCM_SSAHASNP,TISHKOFF,20.966024
ETFAchr157652327376523274rs76155326+AA/Gsingleintron21000GENOMES,BUSHMAN,20.975688
ETFAchr157652361976523620rs76403342+CA/Csingleintron51000GENOMES,BUSHMAN,CLINSEQ_SNP,NHLBI-ESP,TISHKOFF,20.025263
ETFAchr157652377076523771rs62030234+TC/Tsingleintron61000GENOMES,BCMHGSC_JDW,BL,ENSEMBL,NHLBI-ESP,SSMP,20.057798
ETFAchr157652405876524059rs111591775+TG/Tsingleintron31000GENOMES,BUSHMAN,TISHKOFF,20.031207
ETFAchr157652413876524139rs76505232+AA/Tsingleintron11000GENOMES,20.988240
ETFAchr157652444976524450rs2469536+CC/Tsingleintron221000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.021806
ETFAchr157652464376524644rs4886784+TG/Tsingleintron81000GENOMES,BGI,COMPLETE_GENOMICS,GMI,ILLUMINA-UK,PERLEGEN,TISHKOFF,WI_SSAHASNP,20.350688
ETFAchr157652522276525223rs77358466+GA/Gsingleintron21000GENOMES,TISHKOFF,20.027439
ETFAchr157652525776525258rs76200311+TC/Tsingleintron51000GENOMES,BCM-HGSC-SUB,GMI,ILLUMINA,SSMP,20.023934
ETFAchr157652542576525426rs7177923+GA/Gsingleintron141000GENOMES,ABI,BCM-HGSC-SUB,BCM_SSAHASNP,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,20.361261
ETFAchr157652583276525833rs145567147+GC/Gsingleintron21000GENOMES,TISHKOFF,20.030762
ETFAchr157652640976526410rs16968016+CC/Gsingleintron81000GENOMES,BGI,HGSV,ILLUMINA,ILLUMINA-UK,PERLEGEN,SSMP,TISHKOFF,20.951419
ETFAchr157652690676526907rs2456058-TA/Gsingleintron211000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.018679
ETFAchr157652691176526912rs2456057-GC/Gsingleintron191000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,SC_JCM,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.409112
ETFAchr157652708476527085rs78538242+TC/Tsingleintron21000GENOMES,TISHKOFF,20.038328
ETFAchr157652762976527630rs8033494+GA/Gsingleintron131000GENOMES,ABI,BCM-HGSC-SUB,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,GMI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,SSMP,TISHKOFF,WI_SSAHASNP,20.346413
ETFAchr157652795476527955rs4886484+GC/Gsingleintron181000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.429201
ETFAchr157652804076528041rs79095910+AA/Csingleintron31000GENOMES,GMI,SSMP,20.973455
ETFAchr157652815976528160rs8033926+AA/Gsingleintron31000GENOMES,TISHKOFF,WI_SSAHASNP,20.963790
ETFAchr157652883076528831rs12595211+CC/Tsingleintron171000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,KRIBB_YJKIM,PERLEGEN,SSAHASNP,SSMP,TISHKOFF,20.653198
ETFAchr157652903376529034rs111849590+GA/Gsingleintron31000GENOMES,BUSHMAN,TISHKOFF,20.025700
ETFAchr157652904776529048rs62030235+GC/Gsingleintron41000GENOMES,BCMHGSC_JDW,ENSEMBL,SSMP,20.041284
ETFAchr157652947876529479rs199935072+T-/Tdeletionintron11000GENOMES,20.014692
ETFAchr157652972276529723rs2176622-AC/Tsingleintron211000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.978161
ETFAchr157653010276530103rs57182285+GC/Gsingleintron121000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PJP,SSMP,TISHKOFF,20.324634
ETFAchr157653021676530217rs77022998+AA/Tsingleintron11000GENOMES,20.985192
ETFAchr157653026676530267rs2460143-CG/Tsingleintron211000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.032860
ETFAchr157653043376530434rs117556108+AA/Csingleintron21000GENOMES,SSMP,20.978677
ETFAchr157653083976530840rs2456056-TA/Gsingleintron211000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PERLEGEN,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,WUGSC_SSAHASNP,20.019985
ETFAchr157653144976531450rs11072579+CC/Tsingleintron141000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PJP,SSMP,TISHKOFF,20.655547
ETFAchr157653151976531520rs4886485+AA/Csingleintron141000GENOMES,ABI,BCM-HGSC-SUB,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,PERLEGEN,PJP,SSAHASNP,SSMP,WI_SSAHASNP,20.704656
ETFAchr157653164076531641rs57634299+CC/Gsingleintron51000GENOMES,BGI,HGSV,ILLUMINA-UK,SSMP,20.948624
ETFAchr157653166076531661rs2460142-GC/Tsingleintron51000GENOMES,BUSHMAN,ILLUMINA-UK,SC_JCM,TISHKOFF,20.935839
ETFAchr157653266976532670rs75830587+TC/Tsingleintron31000GENOMES,ILLUMINA,TISHKOFF,20.026110
ETFAchr157653284476532845rs2460141-GC/Gsingleintron201000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.097826
ETFAchr157653351576533516rs117181475+CC/Tsingleintron21000GENOMES,ILLUMINA,20.989556
ETFAchr157653391676533917rs11637855+GA/Gsingleintron91000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,CSHL-HAPMAP,ENSEMBL,GMI,SSMP,TISHKOFF,20.309808
ETFAchr157653406176534062rs147396188+GA/Gsingleintron21000GENOMES,SSMP,20.061983
ETFAchr157653412076534121rs188134178+CC/Tsingleintron21000GENOMES,TISHKOFF,20.971534
ETFAchr157653418276534183rs114463047+AA/Tsingleintron11000GENOMES,20.964721
ETFAchr157653561176535611rs139381703+--/Ainsertionintron51000GENOMES,BILGI_BIOE,GMI,LUNTER,SSMP,20.680441
ETFAchr157653569576535696rs5012144+CC/Tsingleintron111000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,DEVINE_LAB,GMI,ILLUMINA-UK,PERLEGEN,SSMP,TISHKOFF,20.650172
ETFAchr157653574276535743rs2456070+CC/Tsingleintron91000GENOMES,BUSHMAN,COMPLETE_GENOMICS,GMI,ILLUMINA-UK,PERLEGEN,SC_JCM,SSMP,TISHKOFF,20.885568
ETFAchr157653590276535903rs59783688+C-/Cdeletionintron61000GENOMES,BILGI_BIOE,GMI,HGSV,LUNTER,SSMP,20.309917
ETFAchr157653592276535923rs114566411+CC/Tsingleintron11000GENOMES,20.974303
ETFAchr157653597376535974rs60017340+TC/Tsingleintron81000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,SSMP,20.314390
ETFAchr157653615776536157rs199573968+--/Ainsertionintron11000GENOMES,20.947658
ETFAchr157653616176536161rs150900759+--/Ainsertionintron21000GENOMES,BL,20.468779
ETFAchr157653616476536164rs71140202+--/Cinsertionintron61000GENOMES,BILGI_BIOE,BUSHMAN,GMI,HUMANGENOME_JCVI,LUNTER,20.584785
ETFAchr157653633676536337rs2456071+CC/Tsingleintron121000GENOMES,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SC_JCM,SSAHASNP,SSMP,20.376884
ETFAchr157653650576536506rs60290059+GA/Gsingleintron111000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PJP,SSMP,20.347527
ETFAchr157653665076536651rs62030240+AA/Tsingleintron51000GENOMES,BCMHGSC_JDW,ENSEMBL,SSMP,TISHKOFF,20.938532
ETFAchr157653747576537476rs77387260+CC/Tsingleintron41000GENOMES,COMPLETE_GENOMICS,GMI,SSMP,20.950000
ETFAchr157653840076538401rs76518305+CC/Tsingleintron21000GENOMES,TISHKOFF,20.964721
ETFAchr157653845876538459rs77633900+GC/Gsingleintron31000GENOMES,GMI,SSMP,20.050868
ETFAchr157653898976538990rs56313024+GC/Gsingleintron61000GENOMES,BCMHGSC_JDW,BL,HGSV,SSMP,TISHKOFF,20.068411
ETFAchr157653948976539490rs2244050+GA/Gsingleintron211000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.972485
ETFAchr157653983776539838rs4886787+CC/Gsingleintron141000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PJP,SSMP,TISHKOFF,WI_SSAHASNP,20.663336
ETFAchr157653994176539941rs202207851+--/Tinsertionintron11000GENOMES,20.984389
ETFAchr157654023076540231rs11072580+GA/Gsingleintron171000GENOMES,ABI,BCM-HGSC-SUB,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,20.419636
ETFAchr157654059776540598rs116241547+TC/Tsingleintron21000GENOMES,TISHKOFF,20.035714
ETFAchr157654110076541101rs6495197+CC/Tsingleintron121000GENOMES,ABI,BCMHGSC_JDW,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,PJP,SC_JCM,SSMP,TISHKOFF,WI_SSAHASNP,20.647623
ETFAchr157654122476541224rs200384853+--/Ainsertionintron21000GENOMES,GMI,20.803949
ETFAchr157654162576541626rs192838995+CA/Csingleintron11000GENOMES,20.027089
ETFAchr157654187476541875rs186642524+CC/Tsingleintron11000GENOMES,20.986226
ETFAchr157654211376542114rs12438741+CA/Csingleintron141000GENOMES,ABI,BCM-HGSC-SUB,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SSAHASNP,SSMP,TISHKOFF,20.397448
ETFAchr157654256376542563rs11445780+--/Ainsertionintron101000GENOMES,BILGI_BIOE,BUSHMAN,DEVINE_LAB,GMI,HGSV,HUMANGENOME_JCVI,LUNTER,PJP,SSMP,20.378552
ETFAchr157654261876542619rs117800361+CC/Tsingleintron21000GENOMES,ILLUMINA,20.968668
ETFAchr157654287976542880rs78529875+GA/Gsingleintron31000GENOMES,BUSHMAN,COMPLETE_GENOMICS,20.043080
ETFAchr157654390976543910rs2469548-AG/Tsingleintron201000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.622567
ETFAchr157654394376543944rs11634472+CC/Tsingleintron141000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PERLEGEN,SSMP,TISHKOFF,20.649183
ETFAchr157654412376544124rs16968032+AA/Gsingleintron51000GENOMES,BGI,GMI,PERLEGEN,SSMP,20.969438
ETFAchr157654499976545000rs114430298+GA/Gsingleintron21000GENOMES,TISHKOFF,20.033101
ETFAchr157654584376545844rs2456072+AA/Gsingleintron121000GENOMES,BCMHGSC_JDW,BUSHMAN,ENSEMBL,GMI,HGSV,ILLUMINA,ILLUMINA-UK,PJP,SC_JCM,SSMP,TISHKOFF,20.830008
ETFAchr157654602076546021rs2247488+CC/Tsingleintron201000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.021789
ETFAchr157654671476546715rs76915335+CC/Tsingleintron21000GENOMES,SSMP,20.988251
ETFAchr157654673076546731rs114031114+CC/Gsingleintron11000GENOMES,20.988676
ETFAchr157654693276546933rs1914816-GC/Tsingleintron131000GENOMES,ABI,BCMHGSC_JDW,BUSHMAN,ENSEMBL,GMI,ILLUMINA,ILLUMINA-UK,PERLEGEN,SC_JCM,SSMP,TISHKOFF,TSC-CSHL,30.814407
ETFAchr157654741776547418rs118119371+CC/Gsingleintron31000GENOMES,GMI,SSMP,20.971715
ETFAchr157654794676547947rs7167004+TC/Tsingleintron121000GENOMES,ABI,BCMHGSC_JDW,BCM_SSAHASNP,BL,CSHL-HAPMAP,ENSEMBL,HGSV,PERLEGEN,PJP,SSMP,TISHKOFF,20.077532
ETFAchr157654813676548137rs59573516+AA/Gsingleintron41000GENOMES,HGSV,ILLUMINA,TISHKOFF,20.986934
ETFAchr157654857876548579rs7166675+AA/Gsingleintron41000GENOMES,BCM_SSAHASNP,HGSV,TISHKOFF,20.964711
ETFAchr157654862476548625rs2456073+TG/Tsingleintron181000GENOMES,ABI,BCM-HGSC-SUB,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PJP,SC_JCM,SSAHASNP,20.928832
ETFAchr157654953176549532rs2469546-CA/Gsingleintron191000GENOMES,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.972534
ETFAchr157654953476549535rs72736875+AA/Gsingleintron11000GENOMES,20.984848
ETFAchr157654980076549801rs138659405+AA/Gsingleintron31000GENOMES,BL,SSMP,20.940771
ETFAchr157655006376550064rs4592616+GA/Gsingleintron101000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,COMPLETE_GENOMICS,GMI,HGSV,SC_JCM,SSMP,TISHKOFF,20.305225
ETFAchr157655027476550275rs111231955+AA/Csingleintron41000GENOMES,BCM-HGSC-SUB,GMI,SSMP,20.693756
ETFAchr157655093276550933rs117050622+GA/Gsingleintron31000GENOMES,GMI,ILLUMINA,20.053090
ETFAchr157655093776550938rs2469545-CA/Gsingleintron241000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PJP,SC_JCM,SC_SNP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.978219
ETFAchr157655097276550973rs11636851+CC/Tsingleintron161000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,SSMP,TISHKOFF,20.665261
ETFAchr157655169476551695rs111734384+AA/Gsingleintron,ncRNA41000GENOMES,BUSHMAN,ILLUMINA,TISHKOFF,20.965138
ETFAchr157655177676551777rs116240154+GA/Gsingleintron,ncRNA21000GENOMES,ILLUMINA,20.010453
ETFAchr157655185176551852rs12913096+GA/Gsingleintron,ncRNA161000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILLUMINA,KRIBB_YJKIM,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,20.344171
ETFAchr157655197176551972rs76319667+GA/Gsingleintron,ncRNA21000GENOMES,ENSEMBL,20.039908
ETFAchr157655248676552486rs199562413+--/Cinsertionintron,ncRNA11000GENOMES,20.969697
ETFAchr157655333276553333rs62030244+CC/Tsingleintron,near-gene-571000GENOMES,BCMHGSC_JDW,BL,COMPLETE_GENOMICS,ENSEMBL,SSMP,TISHKOFF,20.873052
ETFAchr157655349876553499rs62030245+CC/Gsingleintron,near-gene-591000GENOMES,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,ENSEMBL,GMI,ILLUMINA-UK,SSMP,TISHKOFF,20.682234
ETFAchr157655358776553588rs62030246+GA/Gsingleintron,near-gene-581000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,ENSEMBL,GMI,ILLUMINA-UK,SSMP,TISHKOFF,20.306141
ETFAchr157655378976553790rs35831705+CC/Tsingleintron,near-gene-5101000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,ENSEMBL,GMI,ILLUMINA-UK,SSMP,TISHKOFF,20.690018
ETFAchr157655388976553890rs62027004+CC/Tsingleintron,near-gene-561000GENOMES,BCMHGSC_JDW,BL,ENSEMBL,SSMP,TISHKOFF,20.954587
ETFAchr157655467076554670rs201202605+--/Ainsertionintron31000GENOMES,LUNTER,TISHKOFF,20.952250
ETFAchr157655475476554755rs2460146+CC/Tsingleintron141000GENOMES,ABI,BCMHGSC_JDW,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PJP,SC_JCM,SSMP,TISHKOFF,20.831195
ETFAchr157655478976554790rs12592501+CA/Csingleintron151000GENOMES,ABI,BCM-HGSC-SUB,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,ILLUMINA,KRIBB_YJKIM,PJP,SSAHASNP,SSMP,TISHKOFF,20.359165
ETFAchr157655499076554991rs2938697+TC/Tsingleintron161000GENOMES,BCMHGSC_JDW,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.575785
ETFAchr157655501376555014rs60060261+GA/Gsingleintron31000GENOMES,HGSV,TISHKOFF,20.030303
ETFAchr157655502876555029rs2957035+AA/Tsingleintron171000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.053857
ETFAchr157655542076555421rs72475988+CA/Csingleintron61000GENOMES,BGI,ILLUMINA,ILLUMINA-UK,SSMP,TISHKOFF,20.051835
ETFAchr157655553876555539rs2139190+GC/Gsingleintron171000GENOMES,ABI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PERLEGEN,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.384077
ETFAchr157655559876555599rs2456074+TC/Tsingleintron81000GENOMES,BUSHMAN,COMPLETE_GENOMICS,GMI,ILLUMINA-UK,SC_JCM,SSMP,TISHKOFF,20.117216
ETFAchr157655568776555688rs150863351+GA/Gsingleintron31000GENOMES,GMI,TISHKOFF,20.012856
ETFAchr157655571976555720rs12050896+TC/Tsingleintron121000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,ENSEMBL,GMI,ILLUMINA-UK,PJP,SC_SNP,SSMP,TISHKOFF,20.364896
ETFAchr157655598576555986rs2456075+CC/Tsingleintron121000GENOMES,ABI,BCMHGSC_JDW,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,ILLUMINA-UK,SC_JCM,SSMP,TISHKOFF,20.822374
ETFAchr157655612976556130rs56220133+TC/Tsingleintron61000GENOMES,BL,ENSEMBL,HGSV,SSMP,TISHKOFF,20.056881
ETFAchr157655669876556699rs2404974+TG/Tsingleintron191000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PERLEGEN,PJP,SC_JCM,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.356852
ETFAchr157655747576557476rs2469542-AC/Tsingleintron191000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PJP,SC_JCM,SC_SNP,SSMP,TISHKOFF,20.566938
ETFAchr157655755176557551rs34840661+--/Ginsertionintron21000GENOMES,ABI,20.934343
ETFAchr157655755276557553rs2456076+TG/Tsingleintron191000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PJP,SC_JCM,SC_SNP,SSMP,TISHKOFF,20.544460
ETFAchr157655755476557555rs11856358+CC/Tsingleintron61000GENOMES,BCMHGSC_JDW,BL,CSHL-HAPMAP,ENSEMBL,HGSV,20.944597
ETFAchr157655755476557555rs200473372+C-/Cdeletionintron21000GENOMES,ABI,20.054637
ETFAchr157655789676557897rs77539682+CA/Csingleintron11000GENOMES,20.012631
ETFAchr157655793376557934rs79171859+TC/Tsingleintron31000GENOMES,GMI,SSMP,20.012856
ETFAchr157655814276558143rs11072583+TC/Tsingleintron141000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,20.367229
ETFAchr157655816876558169rs2456077+CC/Tsingleintron211000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.017735
ETFAchr157655849076558491rs11072585+TC/Tsingleintron121000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,CSHL-HAPMAP,ENSEMBL,GMI,ILLUMINA-UK,PJP,SSMP,TISHKOFF,20.325787
ETFAchr157655886976558870rs2456078+TC/Tsingleintron91000GENOMES,BL,BUSHMAN,COMPLETE_GENOMICS,GMI,ILLUMINA-UK,SC_JCM,SSMP,TISHKOFF,20.177574
ETFAchr157655948176559482rs191390770+CC/Tsingleintron11000GENOMES,20.989899
ETFAchr157655960576559606rs114969382+AA/Csingleintron11000GENOMES,20.987369
ETFAchr157655994376559944rs74960895+GG/Tsingleintron41000GENOMES,ENSEMBL,ILLUMINA,SSMP,20.957339
ETFAchr157656026476560265rs34893715+GA/Gsingleintron101000GENOMES,ABI,BL,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SSMP,TISHKOFF,20.381976
ETFAchr157656154376561544rs4886788+CC/Tsingleintron101000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,GMI,HGSV,ILLUMINA-UK,SSMP,TISHKOFF,WI_SSAHASNP,20.677829
ETFAchr157656154476561545rs191803651+GA/Gsingleintron21000GENOMES,SSMP,20.011019
ETFAchr157656211776562118rs2469541-CA/Gsingleintron181000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,SC_JCM,SSMP,TISHKOFF,20.526661
ETFAchr157656218876562189rs78247410+GA/Gsingleintron31000GENOMES,GMI,ILLUMINA,20.016988
ETFAchr157656273776562738rs8042654+TC/Tsingleintron91000GENOMES,AFFY,BL,ILLUMINA,KRIBB_YJKIM,PERLEGEN,SSMP,TISHKOFF,WI_SSAHASNP,20.095269
ETFAchr157656347776563478rs12592222+TC/Tsingleintron51000GENOMES,CSHL-HAPMAP,ENSEMBL,GMI,SSMP,20.031164
ETFAchr157656406676564067rs115292371+GA/Gsingleintron11000GENOMES,20.014373
ETFAchr157656439176564392rs77622645+TC/Tsingleintron31000GENOMES,BUSHMAN,TISHKOFF,20.016055
ETFAchr157656502576565026rs35707798+GC/Gsingleintron111000GENOMES,ABI,BCM-HGSC-SUB,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SSMP,20.387112
ETFAchr157656560276565603rs4886789+GA/Gsingleintron121000GENOMES,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,GMI,ILLUMINA-UK,KRIBB_YJKIM,SSMP,TISHKOFF,WI_SSAHASNP,20.355361
ETFAchr157656571576565716rs145934500+GA/Gsingleintron21000GENOMES,GMI,20.013774
ETFAchr157656593076565931rs114566574+AA/Gsingleintron11000GENOMES,20.973432
ETFAchr157656606876566068rs35093755+--/Ainsertionintron81000GENOMES,ABI,BILGI_BIOE,GMI,HUMANGENOME_JCVI,LUNTER,SSMP,TISHKOFF,20.614679
ETFAchr157656685476566855rs2460160-GA/Csingleintron41000GENOMES,ILLUMINA,NHLBI-ESP,SC_JCM,20.010889
ETFAchr157656713776567138rs75809712+AA/Gsingleintron21000GENOMES,TISHKOFF,20.982578
ETFAchr157656714176567142rs12442266+TC/Tsingleintron161000GENOMES,ABI,BCM-HGSC-SUB,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,20.384784
ETFAchr157656732776567328rs62027007+AA/Gsingleintron61000GENOMES,BCMHGSC_JDW,BL,ENSEMBL,SSMP,TISHKOFF,20.923395
ETFAchr157656739876567399rs182084708+CA/Csingleintron11000GENOMES,20.023875
ETFAchr157656748376567484rs2469539-AC/Tsingleintron71000GENOMES,BUSHMAN,GMI,ILLUMINA-UK,SC_JCM,SSMP,TISHKOFF,20.108468
ETFAchr157656820876568209rs2456027+GA/Gsingleintron121000GENOMES,BUSHMAN,COMPLETE_GENOMICS,GMI,HGSV,ILLUMINA,ILLUMINA-UK,PJP,SC_JCM,SSMP,TISHKOFF,WI_SSAHASNP,20.230238
ETFAchr157656839776568398rs35771066+TA/Tsingleintron91000GENOMES,ABI,BCM-HGSC-SUB,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA,SSMP,20.141812
ETFAchr157656857876568579rs2176623-GC/Tsingleintron181000GENOMES,ABI,AFFY,BCM-HGSC-SUB,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,PJP,SC_JCM,SSMP,TISHKOFF,TSC-CSHL,20.633833
ETFAchr157656879176568792rs55805818+CC/Gsingleintron111000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PJP,SSMP,TISHKOFF,20.684235
ETFAchr157656896476568965rs57505558+GG/Tsingleintron51000GENOMES,COMPLETE_GENOMICS,GMI,HGSV,TISHKOFF,20.652294
ETFAchr157656896576568966rs56215269+TC/Tsingleintron21000GENOMES,HGSV,20.046373
ETFAchr157656897276568973rs60561507+TC/Tsingleintron71000GENOMES,BCMHGSC_JDW,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,TISHKOFF,20.336389
ETFAchr157656897476568977rs199816275+TTT-/TTTdeletionintron21000GENOMES,LUNTER,20.253444
ETFAchr157656897676568977rs55794488+TG/Tsingleintron61000GENOMES,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,TISHKOFF,20.357012
ETFAchr157656915076569151rs72736888+CC/Tsingleintron31000GENOMES,SSMP,TISHKOFF,20.921772
ETFAchr157656946876569469rs115752468+GA/Gsingleintron21000GENOMES,TISHKOFF,20.016115
ETFAchr157656982476569824rs35360285+--/Tinsertionintron51000GENOMES,ABI,GMI,SSMP,TISHKOFF,20.865932
ETFAchr157656991476569915rs62027010+CA/Csingleintron61000GENOMES,BCMHGSC_JDW,BL,ENSEMBL,SSMP,TISHKOFF,20.076606
ETFAchr157657014276570143rs2469538-CA/Gsingleintron71000GENOMES,BUSHMAN,COMPLETE_GENOMICS,GMI,SC_JCM,SSMP,TISHKOFF,20.116812
ETFAchr157657059076570591rs2469537-CA/Gsingleintron171000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.978951
ETFAchr157657084276570843rs2037306-GC/Gsingleintron221000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PERLEGEN,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.031567
ETFAchr157657105276571053rs11072587+AA/Tsingleintron131000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,ILLUMINA-UK,PJP,SSMP,TISHKOFF,20.634305
ETFAchr157657111076571111rs7177769+GC/Gsingleintron31000GENOMES,BCM_SSAHASNP,TISHKOFF,20.012393
ETFAchr157657112376571124rs1850722-CA/Gsingleintron191000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,DEVINE_LAB,ENSEMBL,GMI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SC_JCM,SSMP,TISHKOFF,TSC-CSHL,20.317379
ETFAchr157657136776571368rs59691037+CA/Csingleintron81000GENOMES,BCMHGSC_JDW,BL,ENSEMBL,HGSV,PJP,SSMP,TISHKOFF,20.079817
ETFAchr157657160976571610rs8042255+CC/Tsingleintron141000GENOMES,AFFY,BUSHMAN,COMPLETE_GENOMICS,GMI,HGSV,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SSMP,TISHKOFF,WI_SSAHASNP,20.831241
ETFAchr157657167376571674rs11856470+TG/Tsingleintron91000GENOMES,ABI,BL,CSHL-HAPMAP,ENSEMBL,HGSV,PJP,SSMP,TISHKOFF,20.079140
ETFAchr157657185876571871rs202185977+CCTCCCACTTTGG-/CCTCCCACTTTGGdeletionintron31000GENOMES,LUNTER,SSMP,20.028007
ETFAchr157657298576572986rs78540560+CC/Tsingleintron11000GENOMES,20.973868
ETFAchr157657423176574232rs12898415+CC/Tsingleintron111000GENOMES,ABI,BCM-HGSC-SUB,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,SSAHASNP,TISHKOFF,20.624710
ETFAchr157657462776574628rs2469214+GA/Gsingleintron101000GENOMES,BCM_SSAHASNP,BUSHMAN,GMI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,SC_JCM,SSMP,TISHKOFF,20.172157
ETFAchr157657502076575021rs17458234+CC/Tsingleintron101000GENOMES,BL,BUSHMAN,COMPLETE_GENOMICS,HGSV,ILLUMINA,KRIBB_YJKIM,PERLEGEN,SSMP,TISHKOFF,20.928700
ETFAchr157657505376575054rs2456030+CC/Gsingleintron191000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.021057
ETFAchr157657570876575709rs6495199+GA/Gsingleintron31000GENOMES,BCM_SSAHASNP,WI_SSAHASNP,20.013502
ETFAchr157657605976576060rs78052129+AA/Gsingleintron31000GENOMES,ILLUMINA,NHLBI-ESP,20.968668
ETFAchr157657663376576634rs8040590+CC/Tsingleintron41000GENOMES,COMPLETE_GENOMICS,TISHKOFF,WI_SSAHASNP,20.971560
ETFAchr157657671176576712rs114078184+TA/Tsingleintron21000GENOMES,TISHKOFF,20.027439
ETFAchr157657838376578384rs117401465+CA/Csingleintron41000GENOMES,GMI,ILLUMINA,SSMP,20.023064
ETFAchr157657899676578997rs2456069-CA/Gsingleintron171000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SC_JCM,SSMP,TISHKOFF,20.984268
ETFAchr157657908976579090rs10519134+GA/Gsingleintron91000GENOMES,AFFY,COMPLETE_GENOMICS,ENSEMBL,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,PERLEGEN,SSMP,20.049715
ETFAchr157657923376579234rs2291449+AA/Gsingleintron81000GENOMES,AFFY,COMPLETE_GENOMICS,GMI,KRIBB_YJKIM,PERLEGEN,SSMP,YUSUKE,20.956042
ETFAchr157657928576579286rs116391007+AA/Gsingleintron11000GENOMES,20.973868
ETFAchr157657937776579377rs147918951+--/Tinsertionintron31000GENOMES,LUNTER,TISHKOFF,20.975207
ETFAchr157657953576579536rs11631874+GG/Tsingleintron131000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PJP,SSMP,TISHKOFF,20.669406
ETFAchr157657966376579664rs2469221+TC/Tsingleintron201000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SC_JCM,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.982265
ETFAchr157658052676580527rs8039063+CC/Tsingleintron161000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PJP,SSMP,TISHKOFF,WI_SSAHASNP,20.645585
ETFAchr157658054676580547rs2456068-CA/Gsingleintron181000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PJP,SC_JCM,SSMP,TSC-CSHL,WI_SSAHASNP,20.978169
ETFAchr157658119776581198rs2469549-CA/Gsingleintron201000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.976601
ETFAchr157658136776581368rs62027014+AA/Gsingleintron61000GENOMES,BCMHGSC_JDW,BL,ENSEMBL,SSMP,TISHKOFF,20.922936
ETFAchr157658141776581418rs2456067-GC/Tsingleintron71000GENOMES,COMPLETE_GENOMICS,GMI,ILLUMINA-UK,SC_JCM,SSMP,TISHKOFF,20.883135
ETFAchr157658159176581592rs12908334+CC/Tsingleintron141000GENOMES,ABI,BCM-HGSC-SUB,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SSAHASNP,SSMP,TISHKOFF,20.615712
ETFAchr157658274176582742rs146840833+GA/Gsingleintron21000GENOMES,TISHKOFF,20.016529
ETFAchr157658300776583008rs62027016+TC/Tsingleintron61000GENOMES,BCMHGSC_JDW,BL,ENSEMBL,SSMP,TISHKOFF,20.076606
ETFAchr157658329176583292rs56737606+TC/Tsingleintron111000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILLUMINA-UK,SSMP,TISHKOFF,20.353480
ETFAchr157658378976583789rs200988812+--/AGinsertionintron11000GENOMES,20.989899
ETFAchr157658394676583947rs2460150-CA/Gsingleintron161000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SC_JCM,SC_SNP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.809763
ETFAchr157658404476584065rs201405241+TGGCGCCACTGCACT-/TGGCGCCACTGCAdeletionintron21000GENOMES,SSMP,20.033976
ETFAchr157658468676584686rs3215000+--/Ainsertionintron121000GENOMES,ABI,BILGI_BIOE,BUSHMAN,DEVINE_LAB,GMI,HUMANGENOME_JCVI,LUNTER,PJP,SSMP,TISHKOFF,YUSUKE,20.585243
ETFAchr157658578876585789rs74026416+AA/Gsingleintron31000GENOMES,COMPLETE_GENOMICS,ILLUMINA-UK,20.988543
ETFAchr157658579676585797rs75007725+AA/Gsingleintron11000GENOMES,20.987369
ETFAchr157658633276586332rs11384573+--/Ainsertionintron91000GENOMES,BGI,BILGI_BIOE,DEVINE_LAB,GMI,LUNTER,PJP,SSMP,TISHKOFF,20.648760
ETFAchr157658637976586380rs74843424+TC/Tsingleintron11000GENOMES,20.026568
ETFAchr157658698276586983rs62027018+AA/Csingleintron91000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,GMI,ILLUMINA-UK,SSMP,TISHKOFF,20.646654
ETFAchr157658715776587158rs147769885+GA/Gsingleintron11000GENOMES,20.023875
ETFAchr157658731876587319rs8028504+GC/Gsingleintron131000GENOMES,AFFY,BCM-HGSC-SUB,BGI,COMPLETE_GENOMICS,ENSEMBL,GMI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,SSMP,TISHKOFF,WI_SSAHASNP,20.362699
ETFAchr157658737076587371rs2456066-TA/Gsingleintron91000GENOMES,BUSHMAN,COMPLETE_GENOMICS,GMI,ILLUMINA-UK,PERLEGEN,SC_JCM,SSMP,TISHKOFF,20.884666
ETFAchr157658748676587487rs8029637+TC/Tsingleintron151000GENOMES,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,ENSEMBL,GMI,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SSMP,TISHKOFF,WI_SSAHASNP,20.353825
ETFAchr157658777676587777rs3759853+CC/Tsingleintron161000GENOMES,ABI,BCM-HGSC-SUB,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,YUSUKE,20.631396
ETFAchr157658832176588322rs7173941+GA/Gsingleintron31000GENOMES,BCM_SSAHASNP,TISHKOFF,20.023875
ETFAchr157658834376588347rs199862952+GCGT-/GCGTdeletionintron51000GENOMES,BILGI_BIOE,GMI,LUNTER,SSMP,20.166208
ETFAchr157658834676588347rs2456065-TA/Gsingleintron131000GENOMES,ABI,BCMHGSC_JDW,BCM_SSAHASNP,BL,BUSHMAN,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SC_JCM,SSAHASNP,20.065356
ETFAchr157658880576588806rs72736892+TC/Tsingleintron41000GENOMES,BL,SSMP,TISHKOFF,20.080712
ETFAchr157658885376588854rs11633405+TC/Tsingleintron151000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PERLEGEN,PJP,SSMP,TISHKOFF,20.354631
ETFAchr157658926176589262rs4381566+AA/Gsingleintron161000GENOMES,ABI,BCM-HGSC-SUB,BL,BUSHMAN,COMPLETE_GENOMICS,DEVINE_LAB,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.610858
ETFAchr157658927876589279rs16968083+TC/Tsingleintron141000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILLUMINA,ILLUMINA-UK,PERLEGEN,PJP,SSMP,TISHKOFF,20.340131
ETFAchr157658931576589316rs7179750+AA/Gsingleintron141000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PERLEGEN,PJP,SSMP,TISHKOFF,20.645189
ETFAchr157658949476589495rs7180462+GA/Gsingleintron171000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PJP,SSMP,TISHKOFF,20.349976
ETFAchr157658976676589767rs12907668+AA/Tsingleintron121000GENOMES,ABI,BCM-HGSC-SUB,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SSAHASNP,SSMP,20.621894
ETFAchr157658986676589867rs55910716+AA/Tsingleintron61000GENOMES,BL,BUSHMAN,COMPLETE_GENOMICS,HGSV,SSMP,20.926639
ETFAchr157659022276590223rs116223507+CC/Tsingleintron21000GENOMES,ILLUMINA,20.970383
ETFAchr157659040176590403rs145669299+GA-/GAdeletionintron51000GENOMES,BILGI_BIOE,GMI,LUNTER,SSMP,20.307163
ETFAchr157659040776590408rs146303441+GC/Gsingleintron11000GENOMES,20.010101
ETFAchr157659056476590565rs200388945+G-/Gdeletionintron11000GENOMES,20.010560
ETFAchr157659084976590850rs2456064-GC/Tsingleintron221000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.028082
ETFAchr157659094476590945rs11854972+GA/Gsingleintron81000GENOMES,BCMHGSC_JDW,BL,CSHL-HAPMAP,ENSEMBL,HGSV,SSMP,TISHKOFF,20.073988
ETFAchr157659108576591086rs2469208+CC/Gsingleintron231000GENOMES,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,WUGSC_SSAHASNP,20.120626
ETFAchr157659110976591110rs117143808+CC/Tsingleintron31000GENOMES,GMI,ILLUMINA,20.979112
ETFAchr157659119276591193rs8030454+AA/Gsingleintron111000GENOMES,BCM-HGSC-SUB,BGI,COMPLETE_GENOMICS,GMI,ILLUMINA-UK,PERLEGEN,PJP,SSMP,TISHKOFF,WI_SSAHASNP,20.634573
ETFAchr157659127376591274rs2460159+CC/Gsingleintron221000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SC_JCM,SC_SNP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,WUGSC_SSAHASNP,20.016559
ETFAchr157659135676591357rs115302461+TC/Tsingleintron21000GENOMES,TISHKOFF,20.027003
ETFAchr157659181976591820rs3991794-TA/Gsingleintron141000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,ILLUMINA-UK,SC_JCM,SSMP,TISHKOFF,TSC-CSHL,20.646898
ETFAchr157659188676591887rs3958426-GC/Tsingleintron121000GENOMES,ABI,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,ILLUMINA-UK,SC_JCM,SSMP,TISHKOFF,TSC-CSHL,20.646386
ETFAchr157659204876592049rs73453361+GA/Gsingleintron71000GENOMES,BL,BUSHMAN,COMPLETE_GENOMICS,ILLUMINA,SSMP,TISHKOFF,20.073786
ETFAchr157659266776592668rs60261704+CA/Csingleintron51000GENOMES,BL,HGSV,SSMP,TISHKOFF,20.077815
ETFAchr157659273776592738rs11636278+GC/Gsingleintron91000GENOMES,BCM-HGSC-SUB,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,GMI,ILLUMINA-UK,SSMP,TISHKOFF,20.353346
ETFAchr157659362676593627rs79615818+TC/Tsingleintron21000GENOMES,TISHKOFF,20.027439
ETFAchr157659363976593640rs3915459+GG/Tsingleintron141000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PERLEGEN,SC_JCM,SSMP,TISHKOFF,TSC-CSHL,20.647590
ETFAchr157659365376593654rs3915460+CC/Tsingleintron141000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PERLEGEN,SC_JCM,SSMP,TISHKOFF,TSC-CSHL,20.647210
ETFAchr157659377776593778rs62027019+GA/Gsingleintron61000GENOMES,BCMHGSC_JDW,BL,ENSEMBL,SSMP,TISHKOFF,20.080734
ETFAchr157659387576593876rs3927263+AA/Tsingleintron121000GENOMES,ABI,BCMHGSC_JDW,BGI,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA-UK,SC_JCM,SSMP,TSC-CSHL,20.647894
ETFAchr157659387776593878rs3927264+CC/Tsingleintron111000GENOMES,ABI,BCMHGSC_JDW,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA-UK,SC_JCM,SSMP,TSC-CSHL,20.647894
ETFAchr157659399976594000rs11857880+GA/Gsingleintron71000GENOMES,BCMHGSC_JDW,BL,CSHL-HAPMAP,ENSEMBL,SSMP,TISHKOFF,20.079285
ETFAchr157659459476594595rs74805465+AA/Csingleintron41000GENOMES,COMPLETE_GENOMICS,GMI,SSMP,20.948165
ETFAchr157659491776594918rs59673486+T-/Tdeletionintron61000GENOMES,GMI,HGSV,LUNTER,SSMP,TISHKOFF,20.115243
ETFAchr157659495276594953rs3991793-CG/Tsingleintron151000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PJP,SC_JCM,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.646386
ETFAchr157659516876595169rs80112208+AA/Csingleintron21000GENOMES,GMI,20.971715
ETFAchr157659523876595239rs3991792-GC/Gsingleintron141000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILLUMINA-UK,SC_JCM,SSMP,TISHKOFF,TSC-CSHL,20.647301
ETFAchr157659540376595404rs62027047+GC/Gsingleintron61000GENOMES,BCMHGSC_JDW,COMPLETE_GENOMICS,GMI,SSMP,TISHKOFF,20.352752
ETFAchr157659553876595539rs62027048+TC/Tsingleintron81000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,GMI,SSMP,TISHKOFF,20.351835
ETFAchr157659554876595549rs2456063-TA/Gsingleintron71000GENOMES,COMPLETE_GENOMICS,GMI,SC_JCM,SSMP,TISHKOFF,TSC-CSHL,20.889060
ETFAchr157659555076595551rs12443449+CC/Tsingleintron91000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,GMI,SSMP,TISHKOFF,20.645413
ETFAchr157659571576595716rs2469209+AA/Gsingleintron211000GENOMES,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.026671
ETFAchr157659586076595861rs144886912+T-/Tdeletionintron51000GENOMES,GMI,LUNTER,SSMP,TISHKOFF,20.153811
ETFAchr157659609276596093rs117257475+TC/Tsingleintron21000GENOMES,GMI,20.053090
ETFAchr157659621476596215rs4886486+GC/Gsingleintron131000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,GMI,HGSV,ILLUMINA-UK,PJP,SSMP,TISHKOFF,WI_SSAHASNP,20.351327
ETFAchr157659624976596250rs4886791+CC/Tsingleintron151000GENOMES,ABI,AFFY,BCMHGSC_JDW,BGI,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA,KRIBB_YJKIM,PJP,SSMP,TISHKOFF,WI_SSAHASNP,20.681403
ETFAchr157659648976596490rs4886487+AA/Gsingleintron131000GENOMES,BCM-HGSC-SUB,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PJP,SSMP,TISHKOFF,WI_SSAHASNP,20.647032
ETFAchr157659653276596532rs146031895+--/Ainsertionintron31000GENOMES,LUNTER,TISHKOFF,20.975207
ETFAchr157659669976596700rs4886488+GA/Gsingleintron131000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PERLEGEN,PJP,SSMP,TISHKOFF,WI_SSAHASNP,20.348352
ETFAchr157659705676597057rs2469210+GC/Gsingleintron181000GENOMES,ABI,BCM-HGSC-SUB,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PERLEGEN,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.547969
ETFAchr157659725276597253rs138139478+GA/Gsingleintron21000GENOMES,GMI,20.019743
ETFAchr157659725476597255rs113986711+GA/Gsingleintron21000GENOMES,COMPLETE_GENOMICS,20.010092
ETFAchr157659731576597316rs2456062-AC/Tsingleintron191000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.982216
ETFAchr157659855176598552rs61018254+TC/Tsingleintron81000GENOMES,BCM-HGSC-SUB,BGI,GMI,HGSV,ILLUMINA-UK,SSMP,TISHKOFF,20.352294
ETFAchr157659864276598643rs2456061-AA/Tsingleintron151000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SC_JCM,SSAHASNP,SSMP,20.970252
ETFAchr157659869376598694rs139997620+GA/Gsingleintron11000GENOMES,20.025253
ETFAchr157659891776598918rs11634796+CC/Tsingleintron111000GENOMES,ABI,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,ILLUMINA-UK,SSMP,TISHKOFF,20.670174
ETFAchr157659904076599041rs2956875+AA/Gsingleintron81000GENOMES,BUSHMAN,GMI,HGSV,ILLUMINA-UK,SC_JCM,SSMP,TISHKOFF,20.884793
ETFAchr157659926976599273rs139997371+CTCT-/CTCTdeletionintron21000GENOMES,LUNTER,20.023875
ETFAchr157659939576599396rs79172652+TC/Tsingleintron11000GENOMES,20.024390
ETFAchr157659950076599503rs141739111+TTC-/TTCdeletionintron21000GENOMES,LUNTER,20.010101
ETFAchr157659952476599525rs2460156+GA/Gsingleintron51000GENOMES,ILLUMINA,KRIBB_YJKIM,PERLEGEN,SC_JCM,20.013444
ETFAchr157659960076599601rs2460157+GG/Tsingleintron211000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.017743
ETFAchr157659982876599829rs57149671+C-/Cdeletionintron41000GENOMES,HGSV,LUNTER,SSMP,20.078053
ETFAchr157659989176599892rs2469211+AA/Tsingleintron81000GENOMES,BUSHMAN,COMPLETE_GENOMICS,GMI,ILLUMINA-UK,SC_JCM,SSMP,TISHKOFF,20.885481
ETFAchr157659991576599916rs11634060+TC/Tsingleintron131000GENOMES,ABI,BCM-HGSC-SUB,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PJP,SSMP,TISHKOFF,20.364302
ETFAchr157659999476599994rs139280317+--/Tinsertionintron31000GENOMES,BL,LUNTER,20.910468
ETFAchr157660022176600222rs2460158+AA/Tsingleintron81000GENOMES,BUSHMAN,COMPLETE_GENOMICS,GMI,HGSV,ILLUMINA-UK,SC_JCM,SSMP,20.852096
ETFAchr157660063076600631rs2469572+CC/Gsingleintron201000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.021806
ETFAchr157660085376600854rs73453374+AA/Gsingleintron61000GENOMES,BL,BUSHMAN,COMPLETE_GENOMICS,SSMP,TISHKOFF,20.926214
ETFAchr157660091476600914rs142574858+--/Cinsertionintron31000GENOMES,LUNTER,TISHKOFF,20.975207
ETFAchr157660104876601049rs2469573+TC/Tsingleintron81000GENOMES,BUSHMAN,COMPLETE_GENOMICS,GMI,ILLUMINA-UK,SC_JCM,SSMP,TISHKOFF,20.130952
ETFAchr157660107476601075rs2469212+AA/Csingleintron81000GENOMES,BUSHMAN,COMPLETE_GENOMICS,GMI,ILLUMINA-UK,SC_JCM,SSMP,TISHKOFF,20.866300
ETFAchr157660121576601216rs77197552+AA/Csingleintron11000GENOMES,20.974303
ETFAchr157660151576601516rs2056251-CA/Gsingleintron181000GENOMES,ABI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.543508
ETFAchr157660187076601871rs17361504+AA/Gsingleintron141000GENOMES,AFFY,BCM-HGSC-SUB,BL,BUSHMAN,COMPLETE_GENOMICS,GMI,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,PERLEGEN,PJP,SSMP,TISHKOFF,20.618816
ETFAchr157660204376602044rs78977445+GA/Gsingleintron11000GENOMES,20.013502
ETFAchr157660213076602131rs2469574+TC/Tsingleintron201000GENOMES,AFFY,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,20.965561
ETFAchr157660221176602212rs2404972-GC/Tsingleintron121000GENOMES,AFFY,BCM-HGSC-SUB,BGI,GMI,ILLUMINA,KRIBB_YJKIM,PERLEGEN,SC_JCM,SSMP,TISHKOFF,TSC-CSHL,20.637807
ETFAchr157660234576602346rs2404971-GC/Tsingleintron51000GENOMES,ILLUMINA-UK,SSMP,TISHKOFF,TSC-CSHL,20.872018
ETFAchr157660248976602490rs11631935+GA/Gsingleintron31000GENOMES,CSHL-HAPMAP,ENSEMBL,20.013303
ETFAchr157660261376602618rs150922545+AAACA-/AAACAdeletionintron21000GENOMES,LUNTER,20.016070
ETFAchr157660293676602937rs12439484+AA/Csingleintron141000GENOMES,ABI,BCM-HGSC-SUB,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,ILLUMINA,KRIBB_YJKIM,PERLEGEN,SSMP,TISHKOFF,30.614859
ETFAchr157660316376603164rs56372945+AA/Gsingleintron91000GENOMES,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,ENSEMBL,HGSV,ILLUMINA-UK,SSMP,TISHKOFF,20.869963
ETFAchr157660316876603169rs57217518+TC/Tsingleintron71000GENOMES,BCMHGSC_JDW,ENSEMBL,HGSV,ILLUMINA-UK,SSMP,TISHKOFF,20.103575
ETFAchr157660333876603339rs114715150+CA/Csingleintron21000GENOMES,TISHKOFF,20.027439
ETFAchr157660345676603457rs118111581+CC/Tsingleintron21000GENOMES,ILLUMINA,20.989121
ETFAchr157660361076603611rs3215142+A-/Adeletionintron71000GENOMES,BL,GMI,LUNTER,SSMP,TISHKOFF,YUSUKE,20.292470
ETFAchr157660367876603679rs62027051+GC/Gsingleintron81000GENOMES,BCMHGSC_JDW,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,NHLBI-ESP,SSMP,TISHKOFF,20.132326
IVDchr154069822740698228rs111440850+AA/Gsingleintron31000GENOMES,BUSHMAN,TISHKOFF,20.981643
IVDchr154069880540698805rs112373695+--/Ginsertionintron61000GENOMES,BILGI_BIOE,BUSHMAN,LUNTER,SSMP,TISHKOFF,20.890367
IVDchr154069892340698924rs116696916+GC/Gsingleintron11000GENOMES,20.010017
IVDchr154069897540698976rs73383129+GG/Tsingleintron31000GENOMES,COMPLETE_GENOMICS,TISHKOFF,20.984862
IVDchr154069937240699373rs1984793+CA/Csingleintron221000GENOMES,ABI,AFFY,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,PERLEGEN,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.650148
IVDchr154069972640699727rs80175544+GA/Gsingleintron11000GENOMES,20.010017
IVDchr154069983940699840rs34695403+CC/G/Tsingleintron,missense4APPLERA_GI,ILLUMINA,NHLBI-ESP,OMIM-CURATED-RECORDS,20.986842
IVDchr154069993940699940rs2289331-TA/Gsingleintron201000GENOMES,BCMHGSC_JDW,BGI,BL,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PJP,SSAHASNP,SSMP,TISHKOFF,YUSUKE,20.342334
IVDchr154070002140700022rs10518693+CC/Tsingleintron171000GENOMES,AFFY,BCMHGSC_JDW,BGI,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,20.542650
IVDchr154070006940700070rs76137091+TC/Tsingleintron21000GENOMES,NHLBI-ESP,20.010017
IVDchr154070011940700120rs78272986+GA/Gsingleintron31000GENOMES,ILLUMINA,NHLBI-ESP,20.010453
IVDchr154070048240700483rs68169695+TG/Tsingleintron61000GENOMES,BUSHMAN,COMPLETE_GENOMICS,GMI,SSMP,TISHKOFF,20.108257
IVDchr154070059340700594rs114794219+AA/Tsingleintron11000GENOMES,20.989547
IVDchr154070067440700675rs80084737+GG/Tsingleintron11000GENOMES,20.989983
IVDchr154070076640700767rs16970660+GA/Gsingleintron61000GENOMES,BUSHMAN,GMI,PERLEGEN,SSMP,TISHKOFF,20.085766
IVDchr154070163340701634rs56793772+CC/Gsingleintron51000GENOMES,BUSHMAN,COMPLETE_GENOMICS,HGSV,TISHKOFF,20.981210
IVDchr154070196540701966rs73383135+GA/Gsingleintron61000GENOMES,BUSHMAN,COMPLETE_GENOMICS,GMI,SSMP,TISHKOFF,20.116300
IVDchr154070203740702038rs112391853+TC/Tsingleintron31000GENOMES,BUSHMAN,GMI,20.133028
IVDchr154070203740702037rs202230027+--/Cinsertionintron11000GENOMES,20.858127
IVDchr154070219540702196rs34321039+CC/Tsingleintron61000GENOMES,ABI,ENSEMBL,HUMANGENOME_JCVI,PJP,SSMP,20.964286
IVDchr154070225540702256rs4244578+TC/Tsingleintron141000GENOMES,BCMHGSC_JDW,BCM_SSAHASNP,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.307306
IVDchr154070226940702270rs4924464+CC/Gsingleintron111000GENOMES,BCMHGSC_JDW,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.682068
IVDchr154070228640702287rs4924465+AA/Gsingleintron151000GENOMES,BCMHGSC_JDW,BCM_SSAHASNP,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.254902
IVDchr154070229340702294rs4244579+CC/Tsingleintron131000GENOMES,BCMHGSC_JDW,BCM_SSAHASNP,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,SC_JCM,SSMP,TISHKOFF,WI_SSAHASNP,20.265418
IVDchr154070250840702509rs72733442+TC/Tsingleintron61000GENOMES,BUSHMAN,GMI,ILLUMINA,SSMP,TISHKOFF,20.093034
IVDchr154070260040702601rs74763151+TC/Tsingleintron31000GENOMES,BGI,SSMP,20.011749
IVDchr154070311340703114rs8033938+AA/Gsingleintron81000GENOMES,BCM-HGSC-SUB,COMPLETE_GENOMICS,HGSV,PERLEGEN,PJP,SSMP,WI_SSAHASNP,20.940598
IVDchr154070312240703123rs113720703+AA/Csingleintron41000GENOMES,BUSHMAN,COMPLETE_GENOMICS,TISHKOFF,20.985335
IVDchr154070320040703201rs76063119+CC/Tsingleintron11000GENOMES,20.986934
IVDchr154070321040703211rs9635324+AA/Gsingleintron181000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PERLEGEN,PJP,SC_SNP,SSAHASNP,SSMP,TISHKOFF,20.530116
IVDchr154070324240703243rs73383142+TA/Tsingleintron41000GENOMES,BUSHMAN,COMPLETE_GENOMICS,TISHKOFF,20.014665
IVDchr154070333840703339rs8034416+CC/Tsingleintron211000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,PERLEGEN,PJP,SC_SNP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.348708
IVDchr154070360840703609rs4924466+AA/Gsingleintron191000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA,ILLUMINA-UK,PJP,SC_SNP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.022997
IVDchr154070368940703690rs8039298+GC/Gsingleintron21000GENOMES,WI_SSAHASNP,20.012702
IVDchr154070369440703695rs74011152+AA/Gsingleintron31000GENOMES,ILLUMINA-UK,TISHKOFF,20.983945
IVDchr154070401240704013rs73383148+GG/Tsingleintron41000GENOMES,BUSHMAN,COMPLETE_GENOMICS,TISHKOFF,20.985335
IVDchr154070439340704394rs12440317+GA/Gsingleintron121000GENOMES,ABI,BCMHGSC_JDW,BGI,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,ILLUMINA,KRIBB_YJKIM,PERLEGEN,SSMP,20.224439
IVDchr154070459640704597rs74659386+CC/Tsingleintron21000GENOMES,TISHKOFF,20.986063
IVDchr154070510440705105rs2289330-AC/Tsingleintron201000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PJP,SC_SNP,SSAHASNP,SSMP,TISHKOFF,YUSUKE,20.697005
IVDchr154070515840705159rs2289329-TA/Gsingleintron231000GENOMES,ABI,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,PJP,SC_SNP,SSAHASNP,SSMP,TISHKOFF,YUSUKE,20.550768
IVDchr154070535140705352rs73385108+CC/Tsingleintron41000GENOMES,BUSHMAN,COMPLETE_GENOMICS,TISHKOFF,20.976627
IVDchr154070541640705417rs2289328-GC/Tsingleintron131000GENOMES,ABI,BUSHMAN,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,PERLEGEN,SSMP,TISHKOFF,YUSUKE,20.898093
IVDchr154070574040705741rs73385110+CC/Tsingleintron31000GENOMES,COMPLETE_GENOMICS,TISHKOFF,20.976147
IVDchr154070577440705775rs114297147+CC/Gsingleintron21000GENOMES,TISHKOFF,20.985192
IVDchr154070586340705863rs200207728+--/Tinsertionintron11000GENOMES,20.970615
IVDchr154070587840705882rs148431196+TTTG-/TTTGdeletionintron51000GENOMES,BILGI_BIOE,GMI,LUNTER,SSMP,20.638659
IVDchr154070591040705911rs143235545+AA/Csingleintron21000GENOMES,TISHKOFF,20.986685
IVDchr154070601340706014rs111758723+CC/Tsingleintron31000GENOMES,COMPLETE_GENOMICS,TISHKOFF,20.977982
IVDchr154070610040706101rs113638727+CC/Gsingleintron41000GENOMES,BCM-HGSC-SUB,BL,SSMP,20.941274
IVDchr154070624340706244rs34870475+GC/Gsingleintron61000GENOMES,ABI,ENSEMBL,HUMANGENOME_JCVI,PJP,TISHKOFF,20.019248
IVDchr154070640940706410rs73385112+CC/Gsingleintron31000GENOMES,COMPLETE_GENOMICS,TISHKOFF,20.984862
IVDchr154070654440706545rs73385114+CC/Tsingleintron41000GENOMES,COMPLETE_GENOMICS,ILLUMINA,TISHKOFF,20.975688
IVDchr154070666640706667rs9672893+GC/Gsingleintron71000GENOMES,AFFY,BUSHMAN,COMPLETE_GENOMICS,KRIBB_YJKIM,TISHKOFF,WI_SSAHASNP,20.033282
IVDchr154070745540707456rs875767+CC/Tsingleintron111000GENOMES,ABI,BUSHMAN,COMPLETE_GENOMICS,GMI,ILLUMINA,KRIBB_YJKIM,PERLEGEN,SSMP,TISHKOFF,TSC-CSHL,20.891736
IVDchr154070788340707884rs112852617+TC/Tsingleintron31000GENOMES,BUSHMAN,TISHKOFF,20.013761
IVDchr154070842140708422rs11070270+AA/Gsingleintron181000GENOMES,AFFY,BCMHGSC_JDW,BGI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PJP,SSAHASNP,SSMP,TISHKOFF,20.367098
IVDchr154070845440708455rs113309937+GA/Gsingleintron51000GENOMES,BUSHMAN,ILLUMINA,NHLBI-ESP,TISHKOFF,20.050000
IVDchr154070848340708484rs115077254+CC/Tsingleintron61000GENOMES,GMI,ILLUMINA,NHLBI-ESP,SSMP,TISHKOFF,20.973510
IVDchr154070863840708639rs78717580+GA/Gsingleintron11000GENOMES,20.012195
IVDchr154070864340708644rs112366697+CC/Tsingleintron31000GENOMES,BCM-HGSC-SUB,SSMP,20.940383
IVDchr154070870040708701rs111540938+CC/Tsingleintron51000GENOMES,BCM-HGSC-SUB,BL,COMPLETE_GENOMICS,SSMP,20.942202
IVDchr154070933440709335rs149653163+GA/Gsingleintron21000GENOMES,TISHKOFF,20.022498
IVDchr154070935940709360rs111870720+GA/Gsingleintron31000GENOMES,COMPLETE_GENOMICS,TISHKOFF,20.014220
IVDchr154070940340709403rs200004085+--/Ginsertionintron11000GENOMES,20.974747
IVDchr154070942840709429rs112571916+GA/Gsingleintron31000GENOMES,BL,COMPLETE_GENOMICS,20.070183
IVDchr154070957440709575rs148359169+TC/Tsingleintron31000GENOMES,SSMP,TISHKOFF,20.088154
IVDchr154070957840709579rs7172000+CC/Tsingleintron61000GENOMES,BCM_SSAHASNP,BL,COMPLETE_GENOMICS,SSMP,TISHKOFF,20.911468
IVDchr154070968540709686rs2412523+CC/Gsingleintron171000GENOMES,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.341697
IVDchr154071010040710101rs11070271+GG/Tsingleintron151000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,SSAHASNP,SSMP,TISHKOFF,20.482900
IVDchr154071010740710108rs11638033+AA/Tsingleintron141000GENOMES,ABI,BCMHGSC_JDW,BGI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,SSAHASNP,SSMP,TISHKOFF,20.547032
IVDchr154071015040710151rs59636068+CA/Csingleintron41000GENOMES,HGSV,ILLUMINA-UK,TISHKOFF,20.023853
DHODHchr167204282472042825rs3213423+TG/Tsingleintron231000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,YUSUKE,20.875822
DHODHchr167204295972042960rs113616219+GA/Gsingleintron41000GENOMES,BUSHMAN,SSMP,TISHKOFF,20.015138
DHODHchr167204299472042995rs113000464+CA/Csingleintron41000GENOMES,BUSHMAN,SSMP,TISHKOFF,20.015138
DHODHchr167204303872043039rs4788597+CC/Tsingleintron141000GENOMES,BCMHGSC_JDW,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,SSMP,TISHKOFF,WI_SSAHASNP,20.512125
DHODHchr167204328772043288rs182289896+GC/Gsingleintron11000GENOMES,20.033976
DHODHchr167204334372043344rs187293195+GC/Gsingleintron11000GENOMES,20.018366
DHODHchr167204335272043353rs140629801+GC/Gsingleintron21000GENOMES,SSMP,20.039486
DHODHchr167204354572043546rs12149380+GC/Gsingleintron151000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,PJP,SC_SNP,SSAHASNP,SSMP,20.846715
DHODHchr167204400472044005rs2052579-AC/Tsingleintron231000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PJP,SC_JCM,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.969986
DHODHchr167204423772044238rs4788598+GC/Gsingleintron141000GENOMES,BCMHGSC_JDW,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILLUMINA,ILLUMINA-UK,PJP,SSMP,TISHKOFF,WI_SSAHASNP,20.466437
DHODHchr167204449472044495rs61302939+TC/Tsingleintron41000GENOMES,HGSV,ILLUMINA,ILLUMINA-UK,20.018807
DHODHchr167204464672044647rs186136040+TC/Tsingleintron11000GENOMES,20.011938
DHODHchr167204492372044924rs11326070+T-/Tdeletionintron51000GENOMES,DEVINE_LAB,LUNTER,SSMP,TISHKOFF,20.089991
DHODHchr167204518572045186rs2878404-TA/Gsingleintron171000GENOMES,ABI,AFFY,BCMHGSC_JDW,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,ILLUMINA,KRIBB_YJKIM,PJP,SC_JCM,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.598610
DHODHchr167204543672045437rs28483075+GC/Gsingleintron31000GENOMES,COMPLETE_GENOMICS,SSAHASNP,20.031651
DHODHchr167204576272045765rs199731139+GAA-/GAAdeletionintron31000GENOMES,BILGI_BIOE,SSMP,20.020202
DHODHchr167204578672045787rs144600696+TA/Tsingleintron21000GENOMES,WARNICH_LAB,20.010560
DHODHchr167204620072046201rs113393105+GA/Gsingleintron51000GENOMES,BUSHMAN,ILLUMINA,NHLBI-ESP,TISHKOFF,20.014220
DHODHchr167204621072046211rs8057016+GG/Tsingleintron141000GENOMES,AFFY,BUSHMAN,COMPLETE_GENOMICS,HGSV,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,PJP,SSMP,TISHKOFF,WI_SSAHASNP,20.889571
DHODHchr167204626772046268rs1465457-CC/Gsingleintron131000GENOMES,ABI,BCMHGSC_JDW,BL,COMPLETE_GENOMICS,ENSEMBL,GMI,ILLUMINA,PERLEGEN,SC_JCM,SSMP,TISHKOFF,TSC-CSHL,20.405457
DHODHchr167204630472046305rs8058214+TG/Tsingleintron121000GENOMES,AFFY,BUSHMAN,COMPLETE_GENOMICS,HGSV,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,SSMP,TISHKOFF,WI_SSAHASNP,20.110712
DHODHchr167204646072046461rs8061140+AA/Gsingleintron81000GENOMES,BUSHMAN,COMPLETE_GENOMICS,ILLUMINA,ILLUMINA-UK,SSMP,TISHKOFF,WI_SSAHASNP,20.901268
DHODHchr167204647672046477rs8061292+CA/Csingleintron51000GENOMES,COMPLETE_GENOMICS,HGSV,ILLUMINA,WI_SSAHASNP,20.035714
DHODHchr167204667972046680rs111665880+CC/Tsingleintron31000GENOMES,BUSHMAN,TISHKOFF,20.970183
DHODHchr167204706172047064rs67332755+TCT-/TCTdeletionintron41000GENOMES,DEVINE_LAB,LUNTER,SSMP,20.098255
DHODHchr167204710772047109rs66927897+CT-/CTdeletionintron31000GENOMES,DEVINE_LAB,LUNTER,20.031221
DHODHchr167204716972047170rs752434-TA/G/Tsingleintron181000GENOMES,ABI,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILLUMINA,ILLUMINA-UK,PERLEGEN,PJP,SC_JCM,SEQUENOM,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,40.475914
DHODHchr167204728572047286rs4788456+GA/Gsingleintron91000GENOMES,BL,COMPLETE_GENOMICS,GMI,ILLUMINA,PERLEGEN,SSMP,TISHKOFF,WI_SSAHASNP,20.400947
DHODHchr167204749872047499rs16973619+CC/Tsingleintron41000GENOMES,BGI,COMPLETE_GENOMICS,PERLEGEN,20.964260
DHODHchr167204775072047751rs8046916+CC/Gsingleintron211000GENOMES,AFFY,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.058901
DHODHchr167204784872047849rs78383425+CC/Tsingleintron31000GENOMES,BUSHMAN,TISHKOFF,20.970642
DHODHchr167204807972048080rs4788600+GG/Tsingleintron171000GENOMES,AFFY,BCMHGSC_JDW,BCM_SSAHASNP,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SSMP,TISHKOFF,WI_SSAHASNP,20.489891
DHODHchr167204833172048332rs3764310+TC/Tsingleintron201000GENOMES,ABI,AFFY,BCMHGSC_JDW,BL,BUSHMAN,CLINSEQ_SNP,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA,KRIBB_YJKIM,NHLBI-ESP,PERLEGEN,PJP,SSMP,TISHKOFF,WI_SSAHASNP,YUSUKE,20.383809
DHODHchr167204863172048632rs8062895+AA/Gsingleintron141000GENOMES,AFFY,BCMHGSC_JDW,BL,COMPLETE_GENOMICS,GMI,HGSV,ILLUMINA,KRIBB_YJKIM,PERLEGEN,PJP,SSMP,TISHKOFF,WI_SSAHASNP,30.612483
DHODHchr167204875472048755rs190857490+CC/Tsingleintron11000GENOMES,20.988522
DHODHchr167204921172049212rs7184117+GG/Tsingleintron81000GENOMES,BCM_SSAHASNP,BUSHMAN,COMPLETE_GENOMICS,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,SSMP,20.891320
DHODHchr167204962072049621rs3812988-TA/Gsingleintron201000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,YUSUKE,20.109939
DHODHchr167204979772049798rs78356840+GA/Gsingleintron41000GENOMES,BUSHMAN,ILLUMINA,TISHKOFF,20.029358
DHODHchr167204979872049799rs8048262+AA/Tsingleintron111000GENOMES,BCMHGSC_JDW,BL,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,PJP,SSMP,TISHKOFF,WI_SSAHASNP,20.595696
DHODHchr167204988472049887rs150303975+TAT-/TATdeletionintron21000GENOMES,LUNTER,20.028926
DHODHchr167205047972050480rs11864453+CC/Tsingleintron201000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,20.629961
DHODHchr167205050572050506rs73586368+CC/Tsingleintron51000GENOMES,BUSHMAN,COMPLETE_GENOMICS,ILLUMINA,TISHKOFF,20.935410
DHODHchr167205088472050885rs11075914+GC/Gsingleintron191000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,NHLBI-ESP,PJP,SC_SNP,SSAHASNP,SSMP,TISHKOFF,21.000000
DHODHchr167205090372050904rs2278028-GC/Tsingleintron71000GENOMES,CLINSEQ_SNP,GMI,ILLUMINA,NHLBI-ESP,SSMP,YUSUKE,20.976472
DHODHchr167205136872051369rs2278027-AC/Tsingleintron151000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,YUSUKE,20.374829
DHODHchr167205177272051773rs11865639+CC/Gsingleintron61000GENOMES,BUSHMAN,CSHL-HAPMAP,ENSEMBL,SSMP,TISHKOFF,20.980311
DHODHchr167205198272051983rs116851654+TG/Tsingleintron21000GENOMES,ILLUMINA,20.016971
DHODHchr167205200772052008rs34273235+G-/Gdeletionintron101000GENOMES,ABI,BL,DEVINE_LAB,GMI,HUMANGENOME_JCVI,LUNTER,PJP,SSMP,TISHKOFF,20.472018
DHODHchr167205203372052034rs11647889+CC/Gsingleintron51000GENOMES,COMPLETE_GENOMICS,CSHL-HAPMAP,SSMP,TISHKOFF,20.927064
DHODHchr167205229872052299rs75329497+AA/Gsingleintron61000GENOMES,COMPLETE_GENOMICS,GMI,ILLUMINA,SSMP,TISHKOFF,20.834404
DHODHchr167205234772052348rs11648003+AA/Gsingleintron131000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA,PJP,SSAHASNP,SSMP,20.805759
DHODHchr167205236472052365rs8061439+GC/Gsingleintron51000GENOMES,COMPLETE_GENOMICS,ILLUMINA,PERLEGEN,WI_SSAHASNP,20.030603
DHODHchr167205262472052625rs8045316+GA/Gsingleintron61000GENOMES,COMPLETE_GENOMICS,ILLUMINA,KRIBB_YJKIM,PERLEGEN,WI_SSAHASNP,20.044989
DHODHchr167205289072052891rs10048144+CC/Gsingleintron161000GENOMES,ABI,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.454877
DHODHchr167205295672052957rs111993259+CC/Tsingleintron41000GENOMES,BUSHMAN,SSMP,TISHKOFF,20.971088
DHODHchr167205296772052968rs112506454+TG/Tsingleintron21000GENOMES,COMPLETE_GENOMICS,20.032110
DHODHchr167205314072053141rs10048111+TC/Tsingleintron141000GENOMES,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,20.490868
DHODHchr167205391372053914rs113348449+CC/Tsingleintron41000GENOMES,COMPLETE_GENOMICS,SSMP,TISHKOFF,20.888176
DHODHchr167205405172054052rs112128680+GA/Gsingleintron41000GENOMES,COMPLETE_GENOMICS,SSMP,TISHKOFF,20.076147
DHODHchr167205406572054066rs141305769+TG/Tsingleintron31000GENOMES,SSMP,TISHKOFF,20.074839
DHODHchr167205420072054200rs200480530+--/TAinsertionintron11000GENOMES,20.958678
DHODHchr167205461772054618rs76575311+CC/Tsingleintron31000GENOMES,BUSHMAN,TISHKOFF,20.970183
DHODHchr167205492772054928rs118112818+CC/Tsingleintron21000GENOMES,ILLUMINA,20.986510
DHODHchr167205498372054984rs1862752-GA/Csingleintron211000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,NHLBI-ESP,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.482227
DHODHchr167205533572055336rs56387295+CA/Csingleintron61000GENOMES,COMPLETE_GENOMICS,HGSV,ILLUMINA,SSMP,TISHKOFF,20.066972
DHODHchr167205553172055532rs2081223-AG/Tsingleintron201000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.530724
DHODHchr167205564872055649rs2081222-AC/Tsingleintron191000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,TSC-CSHL,20.598993
DHODHchr167205585572055856rs74803415+GA/Gsingleintron61000GENOMES,COMPLETE_GENOMICS,ENSEMBL,GMI,SSMP,TISHKOFF,20.164070
DHODHchr167205638372056384rs114267707+GA/Gsingleintron41000GENOMES,ILLUMINA,NHLBI-ESP,TISHKOFF,20.015244
DHODHchr167205675672056757rs12446480+AA/Gsingleintron181000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,PJP,SSAHASNP,SSMP,TISHKOFF,20.567204
DHODHchr167205728172057282rs2288002-AC/Tsingleintron201000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HUMANGENOME_JCVI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PJP,SSAHASNP,SSMP,TISHKOFF,WI_SSAHASNP,YUSUKE,20.528989
GFERchr1620346602034661rs2075812+TC/Tsingleintron161000GENOMES,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,HGBASE,HGSV,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PJP,SSMP,YUSUKE,20.419587
GFERchr1620352522035253rs34973300+TC/Tsingleintron71000GENOMES,ABI,COMPLETE_GENOMICS,ENSEMBL,HUMANGENOME_JCVI,ILLUMINA,KRIBB_YJKIM,20.044633
GFERchr1620352952035296rs72766612+CA/Csingleintron71000GENOMES,BCM-HGSC-SUB,BL,COMPLETE_GENOMICS,GMI,SSMP,TISHKOFF,20.105963
GFERchr1620353892035390rs2075813+GA/Gsingleintron71000GENOMES,GMI,HGBASE,ILLUMINA,KRIBB_YJKIM,SSMP,YUSUKE,20.032890
GFERchr1620354142035415rs2072684+GC/Gsingleintron211000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BCM_SSAHASNP,BGI,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGBASE,HGSV,HUMANGENOME_JCVI,ILLUMINA-UK,PERLEGEN,PJP,SSAHASNP,SSMP,TISHKOFF,YUSUKE,20.448697
GFERchr1620356132035614rs61572004+GC/Gsingleintron41000GENOMES,BUSHMAN,HGSV,TISHKOFF,20.050871
GFERchr1620357612035762rs72766613+TC/Tsingleintron61000GENOMES,BCM-HGSC-SUB,COMPLETE_GENOMICS,GMI,SSMP,TISHKOFF,20.105963
GFERchr1620357832035784rs72766615+CC/Tsingleintron61000GENOMES,BCM-HGSC-SUB,COMPLETE_GENOMICS,GMI,SSMP,TISHKOFF,20.887615
ACADVLchr1771211047121105rs72839706+CA/Csinglecoding-synon,intron,near-gene-531000GENOMES,ILLUMINA,TISHKOFF,20.020017
ACADVLchr1771215387121539rs41283399+CC/Tsingleintron,near-gene-561000GENOMES,CLINSEQ_SNP,ILLUMINA,NHLBI-ESP,SI_EXO,TISHKOFF,20.980941
ACADVLchr1771217847121785rs2521985+TC/Tsingleintron,near-gene-5181000GENOMES,ABI,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,PJP,SC_JCM,SI_EXO,SSMP,TISHKOFF,20.692197
ACADVLchr1771223397122340rs41283401+GA/Gsingleintron,near-gene-5,untranslated-541000GENOMES,ILLUMINA,SI_EXO,TISHKOFF,20.018712
ACADVLchr1771223767122377rs739669+GA/Gsingleintron,near-gene-5,untranslated-5221000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,KYUGEN,PJP,SI_EXO,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.715864
ACADVLchr1771225617122562rs73976748+GA/Gsingleintron,near-gene-5,untranslated-541000GENOMES,ILLUMINA,ILLUMINA-UK,TISHKOFF,20.071101
ACADVLchr1771226237122624rs2017365+GA/Gsingleintron,near-gene-5,untranslated-5201000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILLUMINA,KRIBB_YJKIM,KYUGEN,PJP,SI_EXO,SSMP,TISHKOFF,TSC-CSHL,WI_SSAHASNP,20.490992
ACADVLchr1771228277122828rs41283403+CC/Tsingleintron,near-gene-5,untranslated-541000GENOMES,ILLUMINA,SI_EXO,TISHKOFF,20.975579
ACADVLchr1771229557122956rs79809891+GA/Gsingleintron,near-gene-5,untranslated-531000GENOMES,ILLUMINA,TISHKOFF,20.027003
ACADVLchr1771230097123010rs79281055+CC/Tsingleintron,near-gene-5,untranslated-521000GENOMES,ILLUMINA,20.986498
ACADVLchr1771232407123240rs421019--A/Gsingleintron,untranslated-52SC_JCM,SEQUENOM,20.750000
ACADVLchr1771233517123352rs2230179+CC/Tsingleintron,missense,untranslated-591000GENOMES,APPLERA_GI,CGAP-GAI,EXOME_CHIP,GENEREVIEWS,ILLUMINA,NHLBI-ESP,TISHKOFF,WICVAR,20.976632
ACADVLchr1771236147123615rs77289756+TG/Tsingleintron,near-gene-521000GENOMES,TISHKOFF,20.033101
ACADVLchr1771238377123838rs28934585+CC/Tsingleintron,near-gene-5,missense,untranslated-5111000GENOMES,APPLERA_GI,CLINSEQ_SNP,EXOME_CHIP,GENEREVIEWS,ILLUMINA,ILLUMINA-UK,NHLBI-ESP,OMICIA,PERLEGEN,SEATTLESEQ,20.970896
ACADVLchr1771245057124506rs77680021+GA/Gsingleintron,near-gene-531000GENOMES,GMI,ILLUMINA,20.041775
ACADVLchr1771246877124688rs8074626+CA/Csingleintron,near-gene-541000GENOMES,COMPLETE_GENOMICS,TISHKOFF,WI_SSAHASNP,20.020015
ACADVLchr1771247907124791rs76640635+AA/Csingleintron,near-gene-521000GENOMES,ENSEMBL,20.975252
ACADVLchr1771248347124836rs60400822+CA-/CAdeletionintron,near-gene-551000GENOMES,HGSV,LUNTER,TISHKOFF,WARNICH_LAB,20.066575
ACADVLchr1771250777125078rs76224236+TC/Tsingleintron,near-gene-531000GENOMES,GMI,ILLUMINA,20.012185
ACADVLchr1771252157125216rs79120091+GA/Gsingleintron,near-gene-531000GENOMES,ILLUMINA,TISHKOFF,20.024826
ACADVLchr1771256537125654rs145589195+TG/Tsingleintron41000GENOMES,CLINSEQ_SNP,NHLBI-ESP,SSMP,20.011512
ACADVLchr1771258267125827rs74562836+CC/Gsingleintron21000GENOMES,ILLUMINA,20.988686
ACADVLchr1771259047125905rs116038940+CC/Tsingleintron31000GENOMES,ILLUMINA,TISHKOFF,20.975610
ACADVLchr1771259357125936rs11870841+GG/Tsingleintron51000GENOMES,CSHL-HAPMAP,ENSEMBL,ILLUMINA,NHLBI-ESP,20.975710
ACADVLchr1771277177127718rs17671352+TC/Tsingleintron,near-gene-5161000GENOMES,ABI,BCM-HGSC-SUB,BCMHGSC_JDW,BL,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,ENSEMBL,GMI,HGSV,ILLUMINA,NHLBI-ESP,PERLEGEN,SSMP,TISHKOFF,20.529262
ACOX1chr177394296273942963rs28590720+TG/Tsingleintron31000GENOMES,SSAHASNP,SSMP,20.039735
ACOX1chr177394297573942976rs2666003+GA/Gsingleintron161000GENOMES,ABI,BCM_SSAHASNP,BGI,BL,BUSHMAN,COMPLETE_GENOMICS,CSHL-HAPMAP,ENSEMBL,GMI,HGSV,ILLUMINA-UK,PJP,SC_JCM,SSMP,TISHKOFF,20.432088
ACOX1chr177394306773943068rs28395254+GA/Gsingleintron31000GENOMES,SSAHASNP,SSMP,20.038493
ACOX1chr177394307073943071rs28496893+TG/Tsingleintron31000GENOMES,SSAHASNP,SSMP,20.038493
ACOX1chr177394334973943350rs2168855-CA/Gsingleintron71000GENOMES,COMPLETE_GENOMICS,GMI,HGSV,SC_JCM,TISHKOFF,TSC-CSHL,20.192308
ACOX1chr177394339773943398rs147326228+GA/Gsingleintron21000GENOMES,SSMP,20.021120
ACOX1chr177394357073943571rs148844589+AA/Gsingleintron11000GENOMES,20.953627
ACOX1chr177394394173943942rs1463486-GC/Tsingleintron101000GENOMES,ABI,BGI,COMPLETE_GENOMICS,GMI,HGSV,SC_JCM,SSMP,TISHKOFF,TSC-CSHL,20.807868
ACOX1chr177394456873944569rs12051891+AA/Csingleintron101000GENOMES,BL,BUSHMAN,GMI,ILLUMINA,ILLUMINA-UK,NHLBI-ESP,SC_SNP,SSMP,TISHKOFF,20.890060
ACOX1chr177394459573944596rs2666005+TG/Tsingleintron111000GENOMES,BGI,BUSHMAN,COMPLETE_GENOMICS,GMI,HGSV,PJP,SC_JCM,SSMP,TISHKOFF,WI_SSAHASNP,20.234218
ACOX1chr177394488973944890rs76447063+CC/Tsingleintron61000GENOMES,BUSHMAN,COMPLETE_GENOMICS,ILLUMINA-UK,SSMP,TISHKOFF,20.927264
ACOX1chr177394493373944937rs200821416+TTTC-/TTTCdeletionintron31000GENOMES,LUNTER,SSMP,20.109275
ACOX1chr177394498573944986rs113620479+GA/Gsingleintron61000GENOMES,BL,BUSHMAN,GMI,SSMP,TISHKOFF,20.108765
ACOX1chr177394523673945237rs8079543+AA/Gsingleintron81000GENOMES,BCM_SSAHASNP,BUSHMAN,COMPLETE_GENOMICS,ILLUMINA-UK,SSMP,TISHKOFF,WI_SSAHASNP,20.926417
ACOX1chr177394552873945529rs8082018+GA/Gsingleintron131000GENOMES,BCM_SSAHASNP,BUSHMAN,COMPLETE_GENOMICS,HGSV,ILLUMINA,ILLUMINA-UK,KRIBB_YJKIM,NHLBI-ESP,PJP,SSMP,TISHKOFF,WI_SSAHASNP,20.093474
ACOX1chr177394574473945745rs9901420+TC/Tsingleintron101000GENOMES,BCM_SSAHASNP,BUSHMAN,CLINSEQ_SNP,COMPLETE_GENOMICS,HGSV,ILLUMINA-UK,PJP,SSMP,TISHKOFF,20.059827
ACOX1chr177394660273946603rs138269925+TG/Tsingleintron21000GENOMES,TISHKOFF,20.016070