chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187188984271889843TG42GENICheterozygous64103266
187188984771889848GA41GENICheterozygous64103267
187190096971900970CT50GENIChomozygous63932760
187189257571892576TG39GENICheterozygous63932755
187189834271898343TG46GENIChomozygous63932756
187189842671898427AT18GENIChomozygous63932757
187189847771898478AT23GENIChomozygous63932758
187190093671900937CT49GENIChomozygous63932759
187190106071901061TG31GENICheterozygous64103268
187190128471901285CG31GENIChomozygous63932761
187190129271901293CG32GENIChomozygous63932762
187190129871901299CG34GENIChomozygous63932763
187190131371901314AG42GENIChomozygous63932764
187190135371901354TG30GENIChomozygous63932765
187190144871901449GT43GENIChomozygous63932766
187190148871901489GT23GENIChomozygous63932767
187192142271921423CT23GENIChomozygous63932768
187194177371941774AG36GENIChomozygous63932773
187194178371941784AG25GENIChomozygous63932774
187194722771947228AT46GENICheterozygous63932775
187194732771947328CT72GENICheterozygous63932776
187195343271953433GT22GENIChomozygous63932780
187195402671954027AG54GENIChomozygous63932782
187197062471970625CA14GENIChomozygous63932784
187197065071970651CA10GENIChomozygous63932785
187198400771984008CT28GENICheterozygous63932786
187199025771990258GT21GENICheterozygous63932787
187203320672033207AT31GENICpossibly homozygous63932788
187205226272052263AG29GENIChomozygous64103269
187198856371988564TG90GENICheterozygous64067773
187208813572088136GA32GENIChomozygous63932791
187209737372097374GA12GENICheterozygous63932793
187210103072101031AG30GENICheterozygous64103270
187213703572137036GT23GENICheterozygous63932797
187218012472180125GA56GENICheterozygous64103271