chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145549879145549880CG24GENICpossibly homozygous112871096
4145551729145551730TC52GENIChomozygous112871097
4145552504145552505AT62GENIChomozygous112871098
4145552904145552905GA72GENIChomozygous112871099
4145553948145553949GT73GENIChomozygous112871100
4145554106145554107TC48GENIChomozygous112871101
4145554224145554225AG41GENIChomozygous112871102
4145554622145554623AC82GENICpossibly homozygous112871103
4145554856145554857GA45GENICpossibly homozygous112871104
4145554939145554940CT62GENIChomozygous112871105
4145554940145554941CG61GENIChomozygous112871106
4145555452145555453TC47GENIChomozygous112871107
4145555501145555502CT52GENIChomozygous112871108
4145555710145555711AG41GENIChomozygous112871109
4145555932145555933CG70GENIChomozygous112871110
4145555985145555986CT63GENIChomozygous112871111