chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106265623362656234CA59GENICpossibly homozygous116614073
106265762462657625CT47GENIChomozygous116939757
106265769962657700TC52GENIChomozygous116614075
106265781762657818AT60GENIChomozygous116614077
106265790162657902CT64GENIChomozygous116939759
106265832562658326AG67GENIChomozygous116939761
106265921862659219GA67GENIChomozygous116939763
106265930262659303CT71GENIChomozygous116939765
106265971662659717GA80GENIChomozygous116890950
106266053962660539CAGACA44GENIChomozygous128823471
106266055562660556G45GENIChomozygous128823472
106266055762660559AG46GENIChomozygous128823473
106266057162660571G47GENIChomozygous128823474
106266058662660586G46GENIChomozygous128823475
106266059562660595G43GENIChomozygous128823476
106266064262660643G33GENIChomozygous128823477
106266110262661103TC62GENIChomozygous116939767
106266139062661391GA63GENIChomozygous116890952
106266139162661392TC60GENIChomozygous116939769
106266148662661487GA57GENIChomozygous116939771
106266156162661562CT56GENIChomozygous116890954
106266157062661571G58GENIChomozygous128823478
106266168262661683GC50GENIChomozygous116614081
106266177962661780G62GENIChomozygous131095446
106266178562661786GA63GENIChomozygous116614085
106266179662661797TC57GENIChomozygous116939773
106266183662661837GT70GENIChomozygous116890966
106266234062662341GT57GENIChomozygous116890968
106266267362662674GA58GENIChomozygous116890970
106266317162663172CT77GENIChomozygous116890972