chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5165379818165379818G16GENIChomozygous128268818
5165379823165379823A17GENIChomozygous128268819
5165379828165379828C17GENIChomozygous128268820
5165379831165379831T18GENIChomozygous128268821
5165379834165379841ACACGTG17GENIChomozygous128268822
5165379863165379864G18GENIChomozygous128268823
5165380708165380709T23GENIChomozygous128268824
5165380770165380771G29GENIChomozygous128268825
5165383985165383985GTGGCCTCTGGCTTGTAGTCCTCCTATGTTAGCTTCCCAAGTGAACCACTAAACTCATCTTTACCTTTGTCCTTTAATGCAAGAGGCCTCTATTAGTCAGGTTTCAGCCTGGAACAAGCCCAGAGCACAATTTTTTTTAAAAGACTTACTCATTTATTATATAT17GENICpossibly homozygous128268827
5165387965165387965C16GENIChomozygous128268828
5165387971165387972T15GENIChomozygous128268829