chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14104503094104503095CT17GENIChomozygous113530470
14104503446104503447CT28GENIChomozygous113530472
14104505339104505340AG41GENIChomozygous113530474
14104506025104506026GC34GENIChomozygous113530476
14104508264104508265CT22GENIChomozygous113530478
14104508785104508786TC10GENICheterozygous118772817
14104508795104508796AG11GENICpossibly homozygous118797627
14104509714104509715TC21GENIChomozygous113530480
14104513549104513550AG20GENIChomozygous113530482
14104519074104519075AC17GENIChomozygous113530484
14104522902104522903CT22GENIChomozygous113530486
14104508802104508803TC9GENIChomozygous118724165