chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14104503094104503095CT53GENIChomozygous113530470
14104503446104503447CT56GENIChomozygous113530472
14104505339104505340AG43GENIChomozygous113530474
14104506025104506026GC34GENICpossibly homozygous113530476
14104508264104508265CT40GENIChomozygous113530478
14104508785104508786TC23GENICheterozygous118772817
14104509714104509715TC39GENIChomozygous113530480
14104513549104513550AG46GENIChomozygous113530482
14104519074104519075AC50GENIChomozygous113530484
14104522902104522903CT34GENIChomozygous113530486
14104508802104508803TC18GENICheterozygous118724165