chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1184368379184368380GA42GENIChomozygous108444513
1184384274184384275CT51GENIChomozygous108444515
1184384832184384833CG45GENIChomozygous108444517
1184385505184385506GT53GENIChomozygous108444519
1184388363184388364AT49GENIChomozygous108444521
1184388570184388571CT40GENIChomozygous108444523
1184388899184388900AG47GENIChomozygous108444525
1184389063184389064TG51GENIChomozygous108444527
1184389332184389333AG35GENICpossibly homozygous108444529
1184390330184390331GA38GENIChomozygous108444531
1184391554184391555TC69GENIChomozygous108444533
1184394235184394236AC41GENIChomozygous108444535
1184394300184394301TC55GENIChomozygous108444537
1184395320184395321TC47GENICpossibly homozygous108444539
1184396147184396148AG33GENIChomozygous108444541
1184397657184397658TC43GENIChomozygous108444543
1184398130184398131AT45GENIChomozygous108444545
1184398343184398344CT36GENIChomozygous108444547
1184398930184398931AG44GENIChomozygous108444549
1184399475184399476AG30GENIChomozygous108444551
1184400094184400095GA48GENIChomozygous108444553
1184401683184401684GA41GENIChomozygous108444555
1184402622184402623GA53GENIChomozygous108444557
1184403049184403050CT54GENIChomozygous108444559
1184403730184403731GA61GENIChomozygous108444561
1184404162184404163AT58GENICpossibly homozygous108444563
1184404326184404327GA39GENIChomozygous108444565
1184407058184407059TG30GENIChomozygous108444567