chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18699529886995299CG33GENIChomozygous109306439
18699531886995319TC33GENIChomozygous109306441
18699543986995440CA34GENIChomozygous120483182
18699574086995741AC40GENIChomozygous109306445
18699641986996420GA10GENIChomozygous109306447
18699680586996806CT25GENIChomozygous109306449
18699714186997142GA35GENIChomozygous109306455
18699730586997306GA48GENIChomozygous109306457
18699762486997625GT36GENIChomozygous109306459
18699803486998035TC49GENIChomozygous109306463
18699862586998626TC35GENIChomozygous108883030
18700022387000224TC43GENIChomozygous109306471
18699912486999125AG44GENIChomozygous109306465
18699936986999370CG41GENIChomozygous109306467
18699991986999920CT41GENIChomozygous109306469
18700073487000735AT29GENIChomozygous108883032
18700249887002499TC33GENIChomozygous109306473
18700254887002549TA42GENIChomozygous109306475
18700262787002628CT39GENIChomozygous109306477
18700269287002693TC43GENIChomozygous108883033
18700306287003063GA25GENIChomozygous109306479
18700428387004284CT37GENIChomozygous109306481
18700429587004296AG36GENICpossibly homozygous109306483
18700450387004504GC38GENIChomozygous109306485
18700505387005054AG44GENIChomozygous109306487
18700541487005415TC32GENIChomozygous109306489
18700569287005693CT31GENIChomozygous109306491