chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1227979505227979506GT18GENIChomozygous61106104
1227980287227980288GA19GENICheterozygous61927284
1227981057227981058C-7GENICpossibly homozygous61106106
1227983180227983181TC3GENICheterozygous61106108
1227990179227990187TTGTTTGT--------1GENIChomozygous61927286
1227990713227990714CT12GENIChomozygous61927288
1227991445227991446GA12GENICheterozygous61106114
1227991543227991544TC7GENIChomozygous61106115