chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2203673127203673128CT33GENIChomozygous74284589
2203679041203679042GA32GENIChomozygous74284598
2203682777203682778CT20GENIChomozygous74284601
2203685383203685384TC32GENIChomozygous74284604
2203686598203686599CG25GENIChomozygous74284607
2203693466203693467CT20GENIChomozygous74284610
2203696272203696273AG37GENIChomozygous74284613
2203696692203696693TC30GENICpossibly homozygous74284616
2203696725203696726TC32GENICpossibly homozygous74284619
2203697641203697642GA29GENIChomozygous74284622
2203700839203700840AG30GENIChomozygous74284625