chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5165379818165379818G19GENIChomozygous128268818
5165379823165379823A19GENIChomozygous128268819
5165379828165379828C19GENIChomozygous128268820
5165379831165379831T20GENIChomozygous128268821
5165379834165379841ACACGTG21GENIChomozygous128268822
5165379863165379864G21GENIChomozygous128268823
5165380708165380709T15GENIChomozygous128268824
5165380770165380771G13GENIChomozygous128268825
5165381957165381957GGGGCTGGGG11GENICpossibly homozygous128268826
5165383985165383985GTGGCCTCTGGCTTGTAGTCCTCCTATGTTAGCTTCCCAAGTGAACCACTAAACTCATCTTTACCTTTGTCCTTTAATGCAAGAGGCCTCTATTAGTCAGGTTTCAGCCTGGAACAAGCCCAGAGCACAATTTTTTTTAAAAGACTTACTCATTTATTATATAT8GENIChomozygous128268827
5165387965165387965C11GENIChomozygous128268828
5165387971165387972T10GENIChomozygous128268829
5165390990165390992CA20GENICheterozygous128268830