chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1167539916167539917CT45GENIChomozygous108357974
1167541094167541095GT52GENICpossibly homozygous109522922
1167547863167547864AT9GENIChomozygous108357976
1167548868167548869GA63GENIChomozygous109522923
1167549475167549476AG57GENIChomozygous108357977
1167550155167550156TC32GENIChomozygous108357978
1167551417167551418GA44GENIChomozygous109522924
1167554389167554390GA32GENIChomozygous109522925
1167554823167554824TA57GENICpossibly homozygous109522926
1167556107167556108AG33GENIChomozygous109343518
1167561952167561953AC50GENIChomozygous109522927
1167562385167562386GA32GENIChomozygous109522928