chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1152073714152073715AG26GENIChomozygous108307786
1152076632152076633AG25GENIChomozygous108307788
1152079462152079463AG27GENIChomozygous108307792
1152082924152082925GA21GENIChomozygous108307794
1152084629152084630CT29GENIChomozygous108307796
1152084660152084661CT32GENIChomozygous108307798
1152085385152085386TC18GENIChomozygous108307800
1152091643152091644GA20GENIChomozygous108307802
1152098135152098136AC22GENIChomozygous108307826
1152098305152098306AT19GENIChomozygous108307828
1152107652152107653CT21GENIChomozygous108307850
1152116358152116359GA37GENIChomozygous108307858
1152116542152116543AG32GENIChomozygous108307860
1152120930152120931CT16GENIChomozygous108307862
1152121030152121031GA18GENIChomozygous108307864
1152121337152121338TC27GENIChomozygous109148519
1152121840152121841GA29GENIChomozygous108307866
1152128612152128613AG23GENIChomozygous108307872
1152130741152130742AG16GENIChomozygous108307874
1152131581152131582TC22GENIChomozygous108307876
1152132022152132023CT26GENIChomozygous108307878
1152132080152132081TC19GENIChomozygous108307880
1152132530152132531CT40GENIChomozygous108307882
1152136129152136130TC22GENIChomozygous108307888
1152136604152136605TC24GENIChomozygous108307890
1152136880152136881GC34GENICpossibly homozygous108307892
1152140600152140601TG11GENIChomozygous108945369
1152142005152142006AG22GENIChomozygous108307894
1152143279152143280GA18GENIChomozygous108307898
1152143818152143819AG19GENIChomozygous108307900
1152144156152144157TC16GENIChomozygous108307902
1152145377152145378CA18GENIChomozygous108307904
1152146467152146468CT25GENIChomozygous108307906
1152147251152147252AG19GENIChomozygous108307908
1152147266152147267CT19GENIChomozygous108307910
1152150883152150884CT24GENIChomozygous108307912
1152152219152152220TG30GENIChomozygous108307914
1152152285152152286CT27GENIChomozygous109148521
1152152570152152571CT19GENIChomozygous108307916
1152152842152152843TC25GENIChomozygous108307918