chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141614109141614110GA49GENIChomozygous109327679
1141614630141614631CA41GENICpossibly homozygous109327682
1141614795141614796CT37GENIChomozygous109327683
1141614809141614810GA33GENIChomozygous109327684
1141614821141614822TC34GENIChomozygous108937013
1141615466141615467CT43GENIChomozygous109327685
1141615671141615672CA44GENIChomozygous109327686
1141616415141616416TA51GENIChomozygous109327687
1141616974141616975CT31GENIChomozygous108937023
1141618503141618504GA41GENIChomozygous109327688
1141621204141621205GA39GENIChomozygous109327689
1141622163141622164TA39GENIChomozygous109327690
1141622662141622663TC46GENIChomozygous108937038
1141622879141622880GA42GENIChomozygous109327691
1141623775141623776GA53GENIChomozygous109327692
1141624426141624427TC29GENIChomozygous108937041
1141630931141630932CT37GENIChomozygous108261386
1141633222141633223AG35GENIChomozygous109327693
1141639623141639623G10GENIChomozygous127438976
1141639624141639624TCAGT10GENIChomozygous127438977
1141639626141639626TAGAGCGCTTGCCTAGC10GENIChomozygous127438978
1141639121141639121TTTTTTTC5GENICheterozygous133368462
1141639629141639629CA8GENIChomozygous127438979
1141654294141654295CA46GENICpossibly homozygous108261404
1141654417141654418G36GENICheterozygous130731704