chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3170366247170366248GA27GENIChomozygous57785507
3170368274170368275GC28GENIChomozygous57785509
3170370191170370192GA40GENIChomozygous57785511
3170370309170370310AG40GENIChomozygous57785513
3170370632170370633AAGACGTAACTT16GENIChomozygous57785515
3170371035170371036AG34GENIChomozygous57785517
3170372927170372928CT37GENIChomozygous57785519
3170373116170373117AG23GENIChomozygous57785521
3170378597170378598TG32INTERGENICpossibly homozygous57785523
3170379760170379761T-6INTERGENICheterozygous57785525
3170379777170379778C-14INTERGENICheterozygous57785527
3170379936170379937TTA16INTERGENIChomozygous57785529