chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191066861710668618CA21GENICheterozygous46059687
191066919910669200GGGA11GENICpossibly homozygous46059688
191066970510669706TC20GENIChomozygous46059690
191066997710669978GA17GENIChomozygous46059691
191067060010670601TG13GENIChomozygous46059693
191067073210670733TG19GENIChomozygous46059694
191067090410670905AG2GENIChomozygous46059695
191067127010671271T-1GENIChomozygous46059696
191067199510671996CT18GENICpossibly homozygous46059698
191067214810672149AG21GENICpossibly homozygous46059699
191067271710672718CT9GENICpossibly homozygous46059702
191067356210673563CT17GENIChomozygous46059704
191067421210674213TC15GENIChomozygous46059705
191067474210674743AG8GENIChomozygous46059706
191067477810674779TC16GENICpossibly homozygous46059707