chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4144400366144400367AC19INTERGENIChomozygous56964690
4144400976144400977C-9INTERGENIChomozygous56964691
4144400988144400990AA--4INTERGENIChomozygous56964692
4144402666144402667GGAT23INTERGENICpossibly homozygous56964694
4144402722144402725GAA---15INTERGENICheterozygous56964695
4144403017144403018TC17INTERGENIChomozygous56964696
4144403964144403965GA5INTERGENIChomozygous56964697
4144403904144403905T-16INTERGENIChomozygous57510242
4144402715144402716GA24INTERGENICheterozygous57948373
4144403305144403306GA19INTERGENIChomozygous57948376
4144411685144411686GC33INTERGENIChomozygous57948379
4144412082144412083AT33INTERGENIChomozygous56964699
4144412223144412224TC28INTERGENIChomozygous56964700
4144412878144412879GA22INTERGENIChomozygous57948382
4144413196144413197CT26INTERGENIChomozygous57948385
4144413742144413743TG30INTERGENIChomozygous57948388
4144414501144414502GA42INTERGENIChomozygous57948391
4144415798144415799TTAC8INTERGENICheterozygous56964702
4144417060144417061GA20INTERGENIChomozygous56964706
4144417105144417106AG17INTERGENIChomozygous56964707
4144417125144417126CT21INTERGENIChomozygous57948394
4144417139144417140TC25INTERGENIChomozygous56964708