chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
730983093098310T-18GENICpossibly homozygous53768096
731001163100117CCTG7GENIChomozygous53768098
731001393100140GGT1GENIChomozygous53768100
731001443100145CCG1GENIChomozygous53768102
731001503100151CCG1GENIChomozygous53768104
731002053100206CCAACA13GENICheterozygous53768105
731006083100609AC17GENICpossibly homozygous53768107
731051303105131TC2GENIChomozygous53768109