chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1227979505227979506GT25GENIChomozygous61106104
1227979659227979660AG18GENIChomozygous61106105
1227981057227981058C-6GENICheterozygous61106106
1227981553227981554CT14GENIChomozygous61106107
1227983180227983181TC15GENIChomozygous61106108
1227983212227983216CTCT----2GENICheterozygous62201971
1227988808227988809TC27GENIChomozygous61106109
1227990178227990179GGTTGGTTGT15GENICpossibly homozygous62549669
1227990620227990621GGA12GENIChomozygous61106110
1227990801227990802CT23GENIChomozygous61106113
1227991445227991446GA13GENIChomozygous61106114
1227991543227991544TC17GENIChomozygous61106115