chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18139338281393388GTGTGT------5GENICheterozygous754600151
18139338481393388GTGT----5GENICheterozygous754600152
18139387281393873TG18GENIChomozygous645841729
18139472081394721AG11GENIChomozygous645841730
18139571581395716AAGTGT7GENICheterozygous754600154
18139571581395716AAGTGTGT7GENICheterozygous754600155
18139606881396070GT--28GENIChomozygous754600156
18139629381396294GC23GENIChomozygous645841731
18139629481396295AC22GENIChomozygous645841732
18139629681396304ATGTTTGG--------23GENIChomozygous754600157
18139630481396305AC21GENIChomozygous645841733
18139630681396307GC21GENIChomozygous645841734
18139630981396315AGATGT------23GENIChomozygous754600158
18139631981396328TCACAACAG---------19GENIChomozygous754600159
18139651381396514T-11GENIChomozygous754600160
18139668681396687GGTTCTTTTT5GENICheterozygous754600161
18139669781396698GT10GENICpossibly homozygous645841735
18139725181397252TG10GENIChomozygous645841736
18139726881397276GTCTGTCT--------7GENICpossibly homozygous754600162
18139756981397570AG26GENIChomozygous645841737
18139820881398209TTG4GENIChomozygous754600165
18139831681398317AG13GENIChomozygous645841738
18139915181399152CT10GENICheterozygous645841739
18139927881399279CCCCCCTCACTGGGGGATTCTAGGCAGGGGCTCTACCACTGAGCCACACCCCCAG2GENIChomozygous754600166
18139980681399807TTTTCC17GENICheterozygous754600167
18139980681399807TTTTCCTTCC17GENICpossibly homozygous754600168