chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57897582978975830CT38GENIChomozygous113885236
57897621078976211CA51GENICpossibly homozygous113885238
57897622878976229GA47GENIChomozygous113885240
57897635878976359GA51GENIChomozygous113885242
57897676878976769TC59GENIChomozygous113885243
57897710478977105TC58GENIChomozygous113885245
57897724478977245GA57GENIChomozygous113885247
57897843478978435CT63GENIChomozygous113885250
57897927578979276CT38GENIChomozygous113885252
57897982178979822TC45GENIChomozygous113885254
57898101978981020AG40GENIChomozygous113885256
57898198878981989CA44GENIChomozygous113885258
57898200378982004TC42GENIChomozygous113885260
57898245778982458TC32GENIChomozygous113885262
57898283778982838CT45GENIChomozygous113885264
57898346578983466TC40GENIChomozygous113885266
57898426478984265CT50GENIChomozygous113885268
57898108078981082GA53GENIChomozygous128201908