chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8118526357118526358GC19GENIChomozygous991356563
8118527316118527317AC8GENIChomozygous991356564
8118527665118527666CT15GENIChomozygous991356565
8118527743118527744TC23GENIChomozygous991356566
8118528101118528102CG15GENIChomozygous991356567
8118528291118528292CT13GENIChomozygous991356568
8118528481118528482GA19GENIChomozygous991356569
8118529024118529025AC20GENIChomozygous991356570
8118529158118529159AG12GENIChomozygous991356571
8118529188118529189AG12GENIChomozygous991356572
8118529280118529281AG19GENIChomozygous991356573
8118529731118529732CA13GENIChomozygous991356574
8118530004118530005CA16GENIChomozygous991356575
8118530694118530695TG16GENIChomozygous991356576
8118531195118531196TG17GENIChomozygous991356577
8118532000118532001CT21GENIChomozygous991356578
8118532272118532273CG20GENIChomozygous991356579
8118533158118533159GA15GENIChomozygous991356580
8118534045118534046TC16GENIChomozygous991356581
8118534207118534208TC19GENIChomozygous991356582
8118534298118534299TC16GENIChomozygous991356583
8118538024118538025TC5GENIChomozygous991356584
8118539595118539596GA21GENIChomozygous991356585
8118539596118539597AT21GENIChomozygous991356586
8118540242118540243GT20GENIChomozygous991356587