chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
152796440227964403AG36GENICpossibly homozygous112667680
152796626527966266CT36GENIChomozygous112667682
152796643227966433TC28GENIChomozygous112667684
152796649127966492TC41GENIChomozygous112667686
152796659927966600GA54GENIChomozygous112667688
152796660927966610CT58GENIChomozygous112667690
152796667027966671GA49GENIChomozygous112667692
152796678927966790CT45GENIChomozygous112667694
152796690027966901AC36GENIChomozygous112667696
152796690627966907CT33GENIChomozygous112667698
152796698727966988GA35GENIChomozygous112667700
152796704127967042AG36GENIChomozygous112667702
152796736127967362GA33GENIChomozygous112667704
152796747727967478TG37GENIChomozygous112667706
152796756727967568AG27GENIChomozygous112667708
152796782527967826CT24GENIChomozygous112667710
152796790027967901CT31GENIChomozygous112667712
152796840027968401CT38GENIChomozygous112667714