chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
730983093098310T-18GENICpossibly homozygous727157784
731001163100117CCTG7GENIChomozygous727157785
731001393100140GGT1GENIChomozygous727157786
731001443100145CCG1GENIChomozygous727157787
731001503100151CCG1GENIChomozygous727157788
731002053100206CCAACA13GENICheterozygous727157789
731006083100609AC17GENICpossibly homozygous596999579
731051303105131TC2GENIChomozygous596999580