chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155479679754796798CT51GENIChomozygous48313016
155479681354796814GA57GENIChomozygous48313017
155479815754798158AG45GENICpossibly homozygous48313018
155479823254798233TC47GENIChomozygous48313019
155479823454798235CT48GENIChomozygous48313020
155479841554798416GC55GENIChomozygous48313021