chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221021234221021235AG45GENIChomozygous108543425
1221024392221024393CA70GENICpossibly homozygous108543427
1221028467221028468CT52GENIChomozygous108543429
1221028620221028621GT62GENIChomozygous108543431
1221031522221031523CT60GENICpossibly homozygous108543433
1221034419221034420AG49GENIChomozygous108543435
1221035372221035373TC51GENIChomozygous108543437
1221039845221039846GA71GENIChomozygous108543439