chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4127329186127329187TC18GENIChomozygous113156579
4127329257127329258AG25GENIChomozygous113156580
4127329436127329437TC11GENIChomozygous113156581
4127330217127330218GA14GENIChomozygous113156582
4127330360127330361CT22GENIChomozygous113156583
4127330511127330512CG5GENIChomozygous113156584
4127330517127330518GA5GENIChomozygous113156585
4127330567127330568GA10GENIChomozygous113156586
4127330612127330613AC20GENIChomozygous113156587
4127330812127330813CT5GENIChomozygous113156588
4127330815127330816TA6GENIChomozygous113156589
4127331402127331403CA12GENIChomozygous113156590
4127331558127331559CT6GENIChomozygous113156591
4127331597127331598AT13GENIChomozygous113156592
4127331697127331698CT18GENIChomozygous113156593
4127331803127331804AT22GENIChomozygous113156594
4127332138127332139CT12GENIChomozygous113156595
4127332628127332629GA20GENIChomozygous113156597
4127332897127332898GT8GENICheterozygous126118623
4127332984127332985AG5GENIChomozygous113156600
4127333002127333003TG5GENIChomozygous113156601
4127333025127333026CT7GENIChomozygous113156602
4127333165127333166TC9GENIChomozygous113156603
4127333217127333218GT9GENIChomozygous113156604
4127333720127333721GT14GENIChomozygous113156605
4127333893127333894AG19GENIChomozygous113156606