chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1201803904201803905T13GENICheterozygous402978866
1201803904201803905TG13GENICpossibly homozygous402978867
1201818365201818366GT20GENICheterozygous402978891
1201818365201818366G20GENICpossibly homozygous402978892
1201819087201819088GT76GENICheterozygous402978893
1201843073201843074TC18GENICheterozygous402978902
1201843073201843074T18GENICheterozygous402978903
1201843075201843076TC18GENICheterozygous402978904
1201843075201843076T18GENICheterozygous402978905
1201819123201819124CT69GENICheterozygous141294103
1201843494201843495T12GENICheterozygous141111240