chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106265623362656234CA31GENIChomozygous116614073
106265762462657625CT23GENIChomozygous116939757
106265769962657700TC19GENIChomozygous116614075
106265781762657818AT24GENICpossibly homozygous116614077
106265790162657902CT32GENIChomozygous116939759
106265832562658326AG20GENIChomozygous116939761
106265921862659219GA24GENIChomozygous116939763
106265930262659303CT42GENIChomozygous116939765
106265971662659717GA33GENIChomozygous116890950
106266057162660571G25GENIChomozygous128823474
106266053962660539CAGACA21GENIChomozygous128823471
106266055562660556G25GENIChomozygous128823472
106266055762660559AG25GENIChomozygous128823473
106266058662660586G23GENIChomozygous128823475
106266059562660595G23GENIChomozygous128823476
106266064262660643G21GENIChomozygous128823477
106266110262661103TC33GENIChomozygous116939767
106266139062661391GA15GENIChomozygous116890952
106266139162661392TC15GENIChomozygous116939769
106266148662661487GA19GENIChomozygous116939771
106266156162661562CT19GENIChomozygous116890954
106266157062661571G19GENIChomozygous128823478
106266168262661683GC19GENIChomozygous116614081
106266178562661786GA22GENIChomozygous116614085
106266179662661797TC21GENIChomozygous116939773
106266183662661837GT22GENIChomozygous116890966
106266234062662341GT30GENIChomozygous116890968
106266267362662674GA31GENIChomozygous116890970
106266317162663172CT23GENIChomozygous116890972
106266177962661780G21GENIChomozygous131095446