chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4148306136148306137AG61GENIChomozygous137229076
4148306725148306726CT59GENIChomozygous137229077
4148306761148306762GA52GENIChomozygous137229078
4148307293148307335TCCTTCCTTCCTTCCCTCCCCTTCCTTCCTTCCTTCCTTCCT29GENIChomozygous136920534
4148307357148307358T22GENICpossibly homozygous136920535
4148308690148308691CT43GENIChomozygous137229079
4148310786148310787CT49GENIChomozygous137229080
4148310839148310840GA55GENIChomozygous137229081
4148311330148311331TA55GENIChomozygous137229082
4148312528148312529TA58GENICpossibly homozygous137229083