chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4179493216179493217GA60GENIChomozygous137280630
4179493528179493529TC55GENIChomozygous137280631
4179493726179493727CT67GENIChomozygous137280632
4179494427179494428AC68GENICpossibly homozygous137280633
4179496113179496114CT27GENIChomozygous137280634
4179496374179496375AC50GENIChomozygous137280635
4179496780179496781CG55GENIChomozygous137280636
4179497153179497154TC48GENIChomozygous137280637
4179500319179500320GA60GENIChomozygous137280638
4179501662179501663GA55GENIChomozygous137280639
4179502830179502831CT61GENIChomozygous137280640
4179503221179503222TA70GENIChomozygous137280641
4179504579179504580GA41GENIChomozygous137280642
4179504943179504944A24GENIChomozygous136933115
4179505536179505537AG54GENIChomozygous137280643
4179510429179510430GA61GENIChomozygous137280644