chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1184368379184368380GA16GENIChomozygous108444513
1184384274184384275CT21GENIChomozygous108444515
1184384832184384833CG27GENIChomozygous108444517
1184385505184385506GT21GENIChomozygous108444519
1184388363184388364AT19GENIChomozygous108444521
1184388570184388571CT26GENIChomozygous108444523
1184388899184388900AG13GENIChomozygous108444525
1184389063184389064TG22GENIChomozygous108444527
1184390330184390331GA22GENIChomozygous108444531
1184391554184391555TC25GENIChomozygous108444533
1184394235184394236AC25GENIChomozygous108444535
1184394300184394301TC21GENIChomozygous108444537
1184395320184395321TC20GENIChomozygous108444539
1184396147184396148AG21GENIChomozygous108444541
1184397657184397658TC27GENIChomozygous108444543
1184398130184398131AT24GENIChomozygous108444545
1184398343184398344CT29GENIChomozygous108444547
1184398930184398931AG19GENIChomozygous108444549
1184399475184399476AG23GENIChomozygous108444551
1184400094184400095GA13GENIChomozygous108444553
1184401683184401684GA18GENIChomozygous108444555
1184402622184402623GA26GENIChomozygous108444557
1184403049184403050CT17GENIChomozygous108444559
1184403730184403731GA17GENIChomozygous108444561
1184404162184404163AT11GENIChomozygous108444563
1184404326184404327GA29GENIChomozygous108444565
1184407058184407059TG19GENIChomozygous108444567