chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191066861710668618CA16GENICheterozygous46059687
191066919910669200GGGA7GENIChomozygous46059688
191066970510669706TC16GENIChomozygous46059690
191066997710669978GA17GENICpossibly homozygous46059691
191067060010670601TG16GENIChomozygous46059693
191067073210670733TG26GENIChomozygous46059694
191067090410670905AG5GENICheterozygous46059695
191067127010671271T-10GENIChomozygous46059696
191067199510671996CT18GENIChomozygous46059698
191067214810672149AG18GENICpossibly homozygous46059699
191067271710672718CT8GENIChomozygous46059702
191067356210673563CT23GENICpossibly homozygous46059704
191067421210674213TC17GENICpossibly homozygous46059705
191067474210674743AG9GENICheterozygous46059706
191067477810674779TC16GENIChomozygous46059707