chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122992195229921953G57GENIChomozygous131491734
122992195529921955CAAGGAT59GENIChomozygous131491735
122992289429922895TC36GENIChomozygous115303208
122992696329926964AT69GENICpossibly homozygous115303212
122992699329926994CG75GENIChomozygous115601696
122992650529926506GA49GENIChomozygous115601692
122992688429926885CA62GENIChomozygous115601694
122992771129927712AG91GENIChomozygous115303214
122992778729927788TG82GENIChomozygous115303216
122992843329928434CT69GENIChomozygous115691827
122992892229928922AC21GENIChomozygous131491736
122992892529928926GC21GENIChomozygous131496007
122992892929928930GC19GENIChomozygous131496008
122992918529929186TA49GENIChomozygous115303222
122992918529929185A47GENIChomozygous131491737
122992970829929709CT76GENICpossibly homozygous115601698