chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7119167024119167025GC13GENICpossibly homozygous54080648
7119171564119171565TC16GENIChomozygous54080649
7119172976119172977GA24GENICpossibly homozygous54750858
7119174257119174258TC20GENIChomozygous54080653
7119174880119174883TTT---1GENIChomozygous54080654
7119178506119178507TC18GENIChomozygous54080658
7119178786119178787CG15GENICpossibly homozygous54080659
7119178787119178788CG15GENICpossibly homozygous54080660
7119178986119178987C-17GENICpossibly homozygous54080661
7119179428119179431TAT---5GENICheterozygous54080662
7119180205119180206C-6GENICheterozygous54232486
7119180586119180587TC8GENICpossibly homozygous54080664
7119181047119181048TTAA14GENICpossibly homozygous54080665
7119181427119181428GA3GENIChomozygous54750860