chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2203673127203673128CT20GENIChomozygous74284589
2203679041203679042GA31GENIChomozygous74284598
2203682777203682778CT25GENIChomozygous74284601
2203685383203685384TC28GENIChomozygous74284604
2203686598203686599CG14GENIChomozygous74284607
2203693466203693467CT35GENIChomozygous74284610
2203696272203696273AG21GENIChomozygous74284613
2203696692203696693TC14GENICpossibly homozygous74284616
2203696725203696726TC16GENICpossibly homozygous74284619
2203697641203697642GA23GENIChomozygous74284622
2203700839203700840AG20GENIChomozygous74284625