chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122456956924569570TG44GENICheterozygous118364986
122457079024570791CT40GENIChomozygous115422252
122457255124572552GA46GENIChomozygous115422254
122457319724573198TC63GENIChomozygous115288371
122457479324574794TG57GENIChomozygous115288375
122457486724574868CA58GENICpossibly homozygous115422256
122457497424574975TG35GENIChomozygous115288377
122457591524575916GA41GENIChomozygous115288379
122457663024576631GA25GENIChomozygous115288383
122457679324576794TC55GENIChomozygous115422258
122457776124577762TC52GENICpossibly homozygous115288385
122457836324578364TC48GENIChomozygous115288387
122457724424577245CT42GENICpossibly homozygous115493093