chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101112112711121128CT31GENIChomozygous116494256
101112127111121272CA46GENICpossibly homozygous116494258
101112223911122240CT39GENICpossibly homozygous116494260
101112306411123065AG46GENIChomozygous116494262
101112426911124270GA30GENIChomozygous116494264
101112436311124364GA41GENIChomozygous116494266
101112535811125359TC55GENIChomozygous116494268
101112551811125519GA77GENIChomozygous116494270
101112926111129262GT19GENICpossibly homozygous117981298
101113008511130086TC39GENIChomozygous116494272
101113148011131481CA33GENICpossibly homozygous116494274