chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1102216776102216777CG28GENIChomozygous61486065
1102216971102216972CCAG14GENIChomozygous61486066
1102217562102217563CA19GENIChomozygous61486067
1102217932102217933AT14GENIChomozygous61486068
1102217988102217989CG22GENIChomozygous61486069
1102218558102218570TAGGTAGGTAGG------------8GENIChomozygous61486070
1102218593102218594GA22GENICheterozygous61486071
1102218668102218669GGA13GENICheterozygous61486073
1102218673102218674CT14GENICheterozygous61486074
1102218677102218678AT14GENICheterozygous61486075
1102219578102219579GA25GENIChomozygous61486076
1102220245102220246AC30GENIChomozygous61486077