chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106600853566008536TC22GENIChomozygous51907672
106600942866009429AG21GENIChomozygous51478966
106601021866010219CCA6GENICheterozygous52382503
106601107466011075AAG28GENIChomozygous51478972
106601430466014306GG--6GENICheterozygous52320353
106601443166014432AAACACAC5GENICheterozygous51478975
106601443166014432AAACACACACAC5GENICheterozygous52382505
106601588666015887AC24GENIChomozygous51907680
106601757366017577AAAC----13GENIChomozygous51478978
106601782866017829GA36GENIChomozygous51907682
106601892466018928CACA----11GENICheterozygous52382507
106601892666018928CA--11GENICheterozygous52382509
106601926866019269AATGTGTGTGTG4GENIChomozygous52382511
106602220666022208TG--11GENICpossibly homozygous51907684
106602278166022785GCCT----9GENIChomozygous52382513
106602283266022833CCCTT15GENICheterozygous51478989
106602283266022833CCCT15GENICheterozygous52461105
106602296666022967AAAAAAAAAC6GENICheterozygous52382515
106602474166024742GGTGTCTCTC2GENICheterozygous52382521
106602491866024919A-11GENIChomozygous52320359
106602678766026788CT21GENIChomozygous51907694
106602682566026826CA23GENIChomozygous51907696
106602770166027702TC29GENIChomozygous51479001
106603013166030132CG26GENIChomozygous51907698