chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5165379818165379818G53GENIChomozygous128268818
5165379823165379823A53GENIChomozygous128268819
5165379828165379828C58GENIChomozygous128268820
5165379831165379831T57GENIChomozygous128268821
5165379834165379841ACACGTG56GENIChomozygous128268822
5165379863165379864G59GENIChomozygous128268823
5165380708165380709T51GENIChomozygous128268824
5165380770165380771G57GENIChomozygous128268825
5165381957165381957GGGGCTGGGG22GENICpossibly homozygous128268826
5165383985165383985GTGGCCTCTGGCTTGTAGTCCTCCTATGTTAGCTTCCCAAGTGAACCACTAAACTCATCTTTACCTTTGTCCTTTAATGCAAGAGGCCTCTATTAGTCAGGTTTCAGCCTGGAACAAGCCCAGAGCACAATTTTTTTTAAAAGACTTACTCATTTATTATATAT42GENICpossibly homozygous128268827
5165387965165387965C23GENIChomozygous128268828
5165387971165387972T20GENIChomozygous128268829
5165390990165390992CA51GENICheterozygous128268830