chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46301367763013678GC13GENIChomozygous122055360
46301534163015342CT66GENIChomozygous112673850
46301701763017018CT46GENIChomozygous112673852
46301880263018803AG65GENIChomozygous112673854
46301975863019759TC65GENIChomozygous112673856
46302223863022239CT54GENIChomozygous112673858
46302415063024151CG47GENIChomozygous119455691
46302512263025123CT55GENIChomozygous119305150
46302633263026333CT73GENIChomozygous112673860
46302804463028045CT61GENICpossibly homozygous112673862
46302905663029057A47GENIChomozygous128041502
46301836763018370CAG53GENIChomozygous128041499
46301950063019500C49GENICpossibly homozygous128041500
46302010863020109A47GENIChomozygous128041501
46303214663032147TC68GENIChomozygous112673864
46303250163032502CA62GENIChomozygous112673866
46303282763032828CG78GENIChomozygous112673868
46303351963033520CA57GENIChomozygous112673870
46303450563034505A55GENICpossibly homozygous128041503
46303465063034651G64GENIChomozygous128041504
46303635263036353TA66GENIChomozygous112673872
46303734263037342G70GENIChomozygous128041505
46303772463037731AACTGCA62GENIChomozygous128041506
46303854263038542AC47GENICpossibly homozygous132601519