chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2057124385712439AG59GENIChomozygous109078982
2057131505713151CG34GENIChomozygous109078984
2057136075713608GA65GENIChomozygous109078986
2057143175714318CA65GENIChomozygous109078988
2057159165715917CT36GENIChomozygous109078990
2057163775716378GA61GENIChomozygous109078992
2057182295718230TG46GENIChomozygous109078994
2057208555720856TG54GENIChomozygous109078996
2057222715722272TC73GENIChomozygous109078998
2057224185722419GT76GENICpossibly homozygous109079000
2057231645723165TA69GENIChomozygous109079002