chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141614630141614631CA17GENIChomozygous109327682
1141614821141614822TC6GENIChomozygous108937013
1141615466141615467CT25GENIChomozygous109327685
1141615671141615672CA21GENIChomozygous109327686
1141616415141616416TA19GENIChomozygous109327687
1141618503141618504GA27GENIChomozygous109327688
1141621204141621205GA13GENIChomozygous109327689
1141622163141622164TA13GENIChomozygous109327690
1141622879141622880GA19GENIChomozygous109327691
1141623775141623776GA9GENIChomozygous109327692
1141624426141624427TC15GENIChomozygous108937041
1141630931141630932CT10GENIChomozygous108261386
1141633222141633223AG16GENIChomozygous109327693
1141642425141642426CG19GENIChomozygous125291254
1141642493141642494CA25GENIChomozygous125291255
1141642532141642533CA26GENIChomozygous125291256
1141642561141642562CT20GENIChomozygous125291257
1141642580141642581CA9GENIChomozygous125291258
1141642602141642603CA17GENIChomozygous125291259
1141642674141642675CA11GENIChomozygous125291260