chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1280635230280635231GT29GENIChomozygous108668379
1280635464280635465GA27GENIChomozygous108668381
1280635598280635599CA35GENICpossibly homozygous108668383
1280635765280635766GA30GENICpossibly homozygous108668384
1280636835280636836CG38GENIChomozygous108668386
1280637051280637052CT35GENIChomozygous108668388
1280637279280637280TG38GENIChomozygous108668390
1280637768280637769CA42GENIChomozygous108668392
1280638105280638106AG31GENIChomozygous108668393
1280639379280639380AG44GENIChomozygous108668395
1280640039280640040CT59GENIChomozygous108668397