chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141614109141614110GA28GENIChomozygous109327679
1141614630141614631CA15GENIChomozygous109327682
1141614795141614796CT19GENIChomozygous109327683
1141614809141614810GA19GENIChomozygous109327684
1141614821141614822TC18GENIChomozygous108937013
1141615466141615467CT20GENIChomozygous109327685
1141615671141615672CA24GENIChomozygous109327686
1141616415141616416TA26GENIChomozygous109327687
1141616974141616975CT29GENIChomozygous108937023
1141618503141618504GA16GENIChomozygous109327688
1141621204141621205GA19GENIChomozygous109327689
1141622163141622164TA23GENIChomozygous109327690
1141622662141622663TC20GENIChomozygous108937038
1141622879141622880GA25GENIChomozygous109327691
1141623775141623776GA29GENIChomozygous109327692
1141624426141624427TC17GENIChomozygous108937041
1141630931141630932CT20GENIChomozygous108261386
1141633222141633223AG14GENIChomozygous109327693
1141654294141654295CA8GENIChomozygous108261404