chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
83230380032303800A29GENIChomozygous132872699
83230385132303852GA39GENIChomozygous116790796
83230471632304717TC69GENIChomozygous116790798
83230695132306952TC67GENICpossibly homozygous116790800
83230779532307796AG54GENIChomozygous116448082
83230838432308385CG56GENIChomozygous116790802
83230865532308656TC57GENIChomozygous116448083
83230933032309331CT33GENIChomozygous116790804
83231078232310783TC53GENICpossibly homozygous116790806
83231191932311920GA61GENIChomozygous116790808
83231196832311969GA80GENIChomozygous116790810
83231538132315382TC48GENICpossibly homozygous116790812
83231562332315624GA49GENIChomozygous116790814
83231960632319607CT46GENIChomozygous116790816
83231987632319877TC53GENIChomozygous116448087
83232411632324117TC48GENIChomozygous116448088
83232428532324285A51GENIChomozygous128579570
83232465732324658TC50GENIChomozygous116448089
83232522832325229AG52GENIChomozygous116790820
83232629132326292CT57GENIChomozygous116790822
83232657532326576AC54GENICpossibly homozygous116790824
83232584832325848GTAT22GENICheterozygous133188188
83232343032323438TCTACTAT42GENICheterozygous133559595