chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109664065996640663AAAT21GENIChomozygous128849657
109664087296640872GG7GENIChomozygous128849658
109664092196640922C7GENIChomozygous128849659
109664094496640944T12GENIChomozygous128849660
109664095196640953GG13GENIChomozygous128849661
109664194096641941TC20GENIChomozygous116691710
109664234496642345AG18GENICpossibly homozygous116691712
109664280896642809AG13GENIChomozygous116691714
109664305596643056GA16GENIChomozygous116691716
109664345096643451AC15GENIChomozygous116691718
109664369596643701TTCTTT15GENIChomozygous128849662
109664819696648197AG25GENIChomozygous116691726
109664568396645684TC11GENIChomozygous116691720
109664720596647206GC19GENIChomozygous116691722
109664751296647513GC11GENIChomozygous116691724
109664891196648915TTTG12GENIChomozygous128849663
109664891996648920TG12GENIChomozygous116691728
109664894796648948A13GENICpossibly homozygous128849664
109664900396649004TA18GENIChomozygous116691730
109664998496649985TC8GENIChomozygous118009982
109665012496650125GA14GENIChomozygous116691732
109665012696650126A14GENIChomozygous128849665
109665012896650129GA14GENIChomozygous117229840
109665039596650396TC15GENIChomozygous116691734
109665099496650996TG16GENIChomozygous128849666
109665100296651003TC17GENIChomozygous117414023
109665117596651176GA25GENIChomozygous116691736
109665130096651301CT17GENIChomozygous117229844
109665161396651614CT21GENIChomozygous116691738
109665167196651672AG28GENIChomozygous116691740
109665172696651727CT31GENIChomozygous116691742
109665192796651928CA16GENIChomozygous116691744
109665222796652228GA11GENIChomozygous116691746
109665242196652422CT16GENIChomozygous117372245
109665321996653220CT22GENIChomozygous116691748
109665329396653294GA22GENIChomozygous116691750
109665362296653623T11GENICpossibly homozygous128849667