chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3170366247170366248GA14GENICpossibly homozygous57785507
3170368274170368275GC14GENIChomozygous57785509
3170370191170370192GA7GENIChomozygous57785511
3170370309170370310AG6GENIChomozygous57785513
3170370632170370633AAGACGTAACTT2GENIChomozygous57785515
3170371035170371036AG13GENIChomozygous57785517
3170372927170372928CT10GENICpossibly homozygous57785519
3170373116170373117AG4GENIChomozygous57785521
3170378597170378598TG13INTERGENICpossibly homozygous57785523
3170378733170378734CCAAA1INTERGENIChomozygous58632189
3170379936170379937TTA8INTERGENIChomozygous57785529