chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134227552042275521CT45GENIChomozygous144928925
134228104742281047A30GENICpossibly homozygous144100549
134228139542281396TC48GENIChomozygous144928926
134228145542281456CT54GENICpossibly homozygous144928927
134228147342281473GACA53GENICpossibly homozygous144924538
134228184142281842CT48GENICpossibly homozygous144928928
134228286742282868AC39GENIChomozygous144928929
134228287942282880C40GENIChomozygous144924539
134228288242282883C35GENICpossibly homozygous144924540
134228330142283302TG57GENIChomozygous144928930
134228347942283480CT83GENIChomozygous144928931
134228389142283892CA67GENICpossibly homozygous144928932
134228452642284527GT46GENIChomozygous144928933
134228485442284855T10GENICheterozygous144924541
134228567542285676AT42GENIChomozygous144928934
134228627742286278CT61GENIChomozygous144928935