chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
86180876461808765T41GENICpossibly homozygous130567639
86180887061808871AG66GENIChomozygous117109433
86181101261811013TC64GENIChomozygous116835023
86181530561815306CA54GENIChomozygous116835027
86181633361816334GA62GENIChomozygous116835029
86181669261816693CT62GENIChomozygous116835031