chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57897582978975830CT52GENIChomozygous113885236
57897621078976211CA63GENIChomozygous113885238
57897622878976229GA61GENIChomozygous113885240
57897635878976359GA58GENIChomozygous113885242
57897676878976769TC61GENIChomozygous113885243
57897710478977105TC62GENIChomozygous113885245
57897724478977245GA41GENIChomozygous113885247
57897843478978435CT64GENICpossibly homozygous113885250
57897927578979276CT46GENIChomozygous113885252
57897982178979822TC64GENIChomozygous113885254
57898101978981020AG56GENICpossibly homozygous113885256
57898198878981989CA55GENIChomozygous113885258
57898200378982004TC55GENIChomozygous113885260
57898245778982458TC45GENIChomozygous113885262
57898283778982838CT61GENIChomozygous113885264
57898346578983466TC53GENIChomozygous113885266
57898426478984265CT46GENIChomozygous113885268