chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
86180877261808773TG26GENIChomozygous116835021
86180887061808871AG22GENIChomozygous117109433
86180950861809509AC12GENIChomozygous117157979
86181101261811013TC22GENICpossibly homozygous116835023
86181470861814709CT34GENIChomozygous117109434
86181530561815306CA19GENIChomozygous116835027
86181633361816334GA25GENIChomozygous116835029
86181669261816693CT44GENIChomozygous116835031