chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3170366247170366248GA34GENIChomozygous57785507
3170368274170368275GC35GENIChomozygous57785509
3170370191170370192GA35GENIChomozygous57785511
3170370309170370310AG37GENIChomozygous57785513
3170370632170370633AAGACGTAACTT35GENIChomozygous57785515
3170371035170371036AG48GENIChomozygous57785517
3170372927170372928CT32GENICpossibly homozygous57785519
3170373116170373117AG44GENIChomozygous57785521
3170378597170378598TG42INTERGENICpossibly homozygous57785523
3170378733170378734CCAAA5INTERGENICheterozygous58632189
3170379760170379761T-17INTERGENICheterozygous57785525
3170379936170379937TTA25INTERGENIChomozygous57785529