chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134227552042275521CT39GENIChomozygous144928925
134228104742281047A40GENICpossibly homozygous144100549
134228139542281396TC38GENIChomozygous144928926
134228145542281456CT43GENIChomozygous144928927
134228147342281473GACA41GENIChomozygous144924538
134228184142281842CT44GENIChomozygous144928928
134228286742282868AC35GENIChomozygous144928929
134228287942282880C31GENIChomozygous144924539
134228288242282883C29GENICpossibly homozygous144924540
134228288242282883CA29GENICheterozygous154811077
134228330142283302TG66GENIChomozygous144928930
134228347942283480CT69GENIChomozygous144928931
134228389142283892CA49GENIChomozygous144928932
134228452642284527GT54GENIChomozygous144928933
134228485442284855T10GENICheterozygous144924541
134228485442284855TG10GENIChomozygous154811078
134228567542285676AT36GENICpossibly homozygous144928934
134228627742286278CT58GENIChomozygous144928935
134228484842284848G9GENICheterozygous148235446