chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8118890556118890557TG14GENIChomozygous117062257
8118890666118890667TC19GENIChomozygous116674810
8118890799118890800TC15GENIChomozygous117062259
8118890941118890942AG21GENIChomozygous117062263
8118890956118890957CT22GENIChomozygous117062265
8118891093118891094AC18GENIChomozygous117062267
8118891448118891449AG17GENIChomozygous117062269
8118891657118891658CT23GENIChomozygous117062271
8118891678118891679CT25GENIChomozygous117062273
8118891804118891805TC22GENIChomozygous117062275
8118891950118891951TA22GENIChomozygous117062277
8118892525118892526GA16GENIChomozygous117062279
8118892603118892604CT25GENIChomozygous116674812
8118892664118892665AG18GENIChomozygous117930465
8118892665118892666CA18GENIChomozygous117930466
8118892697118892698TG17GENIChomozygous117062281
8118892746118892747TC14GENIChomozygous117062283
8118893017118893018CA20GENIChomozygous117062285
8118893235118893236CG12GENIChomozygous117062287
8118893423118893424GA14GENIChomozygous117062289
8118893433118893434TC12GENIChomozygous117062291