chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5165379818165379818G51GENIChomozygous128268818
5165379823165379823A51GENIChomozygous128268819
5165379828165379828C52GENIChomozygous128268820
5165379831165379831T53GENIChomozygous128268821
5165379834165379841ACACGTG57GENIChomozygous128268822
5165379863165379864G49GENIChomozygous128268823
5165380708165380709T60GENIChomozygous128268824
5165380770165380771G63GENIChomozygous128268825
5165381957165381957GGGGCTGGGG23GENIChomozygous128268826
5165383985165383985GTGGCCTCTGGCTTGTAGTCCTCCTATGTTAGCTTCCCAAGTGAACCACTAAACTCATCTTTACCTTTGTCCTTTAATGCAAGAGGCCTCTATTAGTCAGGTTTCAGCCTGGAACAAGCCCAGAGCACAATTTTTTTTAAAAGACTTACTCATTTATTATATAT51GENICpossibly homozygous128268827
5165387965165387965C31GENIChomozygous128268828
5165387971165387972T31GENIChomozygous128268829
5165387988165387989AC29GENICheterozygous131863330
5165387994165387995TC27GENICheterozygous131863331
5165387996165387997AC27GENICheterozygous131863332
5165388002165388003AC24GENICheterozygous131863333