chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1169433733169433734AG25GENIChomozygous108365453
1169435350169435351CG7GENIChomozygous108365457
1169435372169435373GT8GENICpossibly homozygous108365459
1169436227169436228GA16GENIChomozygous108365461
1169436656169436657CT25GENIChomozygous108365463
1169436703169436704CA18GENIChomozygous108365465
1169437695169437696TC14GENIChomozygous108365467
1169437929169437930AC17GENIChomozygous108365469
1169438677169438678GA21GENIChomozygous108365471
1169439553169439554AT20GENIChomozygous108365473
1169439899169439900TC27GENIChomozygous108365475
1169441373169441374AC17GENIChomozygous108365477
1169442256169442257CT21GENIChomozygous108365479
1169442583169442584GC23GENIChomozygous108365481
1169442716169442717CT20GENIChomozygous108365483
1169443412169443413CT20GENIChomozygous108365485
1169444262169444263GA33GENIChomozygous108365487
1169444686169444687TC22GENIChomozygous108365489