chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187478772974787730GT29GENICpossibly homozygous63940491
187479790674797907TG29GENIChomozygous64068047
187479790774797908GT30GENIChomozygous64068048
187479840974798410AC5GENIChomozygous63940493
187479846874798469GT5GENIChomozygous63940495
187482540774825408TC36GENIChomozygous63940505
187493753774937538TC44GENICpossibly homozygous63940531
187493753974937540TC46GENICpossibly homozygous63940533
187493970774939708TC12GENIChomozygous63940555
187493971374939714GC11GENIChomozygous63940557
187493972974939730GT9GENIChomozygous63940559
187493973974939740TC7GENIChomozygous63940561
187493974174939742GC7GENIChomozygous63940563
187493974774939748CA7GENIChomozygous63940565
187493975374939754AC5GENIChomozygous63940567
187493975474939755GT5GENIChomozygous63940569