chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187478772974787730GT19GENICheterozygous63940491
187479790674797907TG34GENIChomozygous64068047
187479790774797908GT35GENIChomozygous64068048
187479840974798410AC9GENIChomozygous63940493
187479846874798469GT12GENIChomozygous63940495
187492977774929778TA2GENIChomozygous64068052
187493753774937538TC32GENICheterozygous63940531
187493753974937540TC34GENICpossibly homozygous63940533
187493970774939708TC14GENIChomozygous63940555
187493971374939714GC12GENIChomozygous63940557
187493972974939730GT11GENIChomozygous63940559
187493973974939740TC10GENIChomozygous63940561
187493974174939742GC10GENIChomozygous63940563
187493974774939748CA10GENIChomozygous63940565
187493975374939754AC8GENIChomozygous63940567
187493975474939755GT8GENIChomozygous63940569
187494091674940917CT18GENIChomozygous63940581
187494094374940944AT22GENIChomozygous64927968