chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47050787970507880TG68GENIChomozygous137079394
47050897870508979GA48GENIChomozygous137079395
47051269770512698CT60GENIChomozygous137079396
47051307270513073GT37GENIChomozygous137079397
47051331770513318CG40GENIChomozygous137079398
47051364870513649CT55GENIChomozygous137079399
47051491270514913CT42GENIChomozygous137079400
47051583370515834AT58GENIChomozygous137079401
47051599670515997CT49GENIChomozygous137079402
47051629470516295GA54GENIChomozygous137079403
47051644670516447CT43GENIChomozygous137079404
47051660670516607CT57GENIChomozygous137079405
47051758370517584TC48GENIChomozygous137079406
47051775470517755CA52GENIChomozygous137079407
47051781670517817GA44GENIChomozygous137079408
47051972170519722AG66GENIChomozygous137079409
47051323770513238G9GENICheterozygous403102993
47051713670517137T30GENICheterozygous403102994
47051713670517137TC30GENICheterozygous403102995
47051323770513238GA9GENICpossibly homozygous140878406
47051322870513230AA9GENICpossibly homozygous136891134
47052216470522164T45GENIChomozygous136891135