chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4127329186127329187TC26GENICpossibly homozygous113156579
4127329257127329258AG19GENICpossibly homozygous113156580
4127329436127329437TC20GENICpossibly homozygous113156581
4127330217127330218GA33GENIChomozygous113156582
4127330360127330361CT31GENICpossibly homozygous113156583
4127330567127330568GA31GENIChomozygous113156586
4127330612127330613AC36GENIChomozygous113156587
4127331402127331403CA27GENIChomozygous113156590
4127331558127331559CT16GENIChomozygous113156591
4127331597127331598AT22GENIChomozygous113156592
4127331803127331804AT20GENICpossibly homozygous113156594
4127332138127332139CT26GENIChomozygous113156595
4127332628127332629GA39GENICpossibly homozygous113156597
4127332971127332972GT23GENIChomozygous113156598
4127332972127332973AT24GENIChomozygous113156599
4127333025127333026CT21GENIChomozygous113156602
4127333217127333218GT18GENICpossibly homozygous113156604
4127333720127333721GT27GENICpossibly homozygous113156605
4127333893127333894AG24GENICpossibly homozygous113156606