chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167472417974724180TC28GENIChomozygous112079456
167472418674724187AT31GENIChomozygous112079458
167472563774725638CT23GENIChomozygous112079460
167473151674731517TC31GENICpossibly homozygous111861651
167473202674732027CT33GENIChomozygous112079462
167473206674732067AG27GENIChomozygous112079464
167473211774732118AG16GENIChomozygous111861653
167473224374732244AG14GENIChomozygous112032774
167473277774732778TC20GENICpossibly homozygous111861659
167473450174734502GT24GENIChomozygous112079466
167473582874735829TC26GENIChomozygous111861665
167473925774739258CT21GENIChomozygous111861673
167474089474740895GT12GENIChomozygous111861680
167474287974742880GC29GENIChomozygous112079468
167474353774743538AG9GENIChomozygous111861682
167473403974734040GA14GENIChomozygous112212834