chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122556378925563790AG19GENIChomozygous115290724
122556559125565592GA23GENIChomozygous115290726
122556717925567180TC19GENIChomozygous115447737
122556747925567480GA20GENICpossibly homozygous115290728
122556884725568848AG7GENIChomozygous115290732
122556898525568986CG10GENIChomozygous115290734
122557057225570573TC12GENIChomozygous115290736
122557077325570774GT19GENIChomozygous115290738
122557088625570887AG11GENIChomozygous115290740
122557095125570952CT23GENIChomozygous115290742
122557122925571230GC11GENIChomozygous115290744
122557243225572433AG15GENIChomozygous115290746
122557523525575236TA25GENIChomozygous115290748
122557584425575845AG19GENIChomozygous115290750
122557628025576281AG37GENIChomozygous115290752
122557645725576458TA21GENIChomozygous115290754
122557762525577626TC17GENIChomozygous115290756
122557837425578375CT16GENIChomozygous115290758
122558769625587697AC13GENIChomozygous115290760
122558772125587722CT17GENIChomozygous115290762
122559134125591342CT11GENIChomozygous115290766
122559216425592165TC16GENIChomozygous115290768
122558955825589559CT30GENIChomozygous115599050
122557503725575038GT17GENICheterozygous115422910
122557503925575040CT13GENICheterozygous115422912
122557801825578019TC2GENIChomozygous115599046
122558275225582753TA25GENIChomozygous115599048