chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108507134585071346A19GENIChomozygous131468059
108507222185072222CT15GENIChomozygous117018743
108507225285072253CT17GENIChomozygous117018744
108507232885072328CCC16GENICpossibly homozygous131468060
108507236185072361T17GENICpossibly homozygous131468061
108507232485072325GA17GENICpossibly homozygous117258168
108507233685072337GA16GENICpossibly homozygous117258170
108507235985072360AT17GENICpossibly homozygous116665116
108508045785080458TC28GENIChomozygous116665120
108508187985081879T13GENIChomozygous128841215
108508279585082796CG21GENIChomozygous116665126
108508392085083921CT17GENIChomozygous117018746