chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1152073714152073715AG19GENIChomozygous108307786
1152076632152076633AG23GENIChomozygous108307788
1152077327152077328CT19GENIChomozygous108307790
1152079462152079463AG18GENIChomozygous108307792
1152082924152082925GA19GENIChomozygous108307794
1152084629152084630CT31GENIChomozygous108307796
1152084660152084661CT30GENIChomozygous108307798
1152085385152085386TC14GENIChomozygous108307800
1152091643152091644GA14GENIChomozygous108307802
1152098135152098136AC30GENIChomozygous108307826
1152098305152098306AT23GENIChomozygous108307828
1152107652152107653CT15GENIChomozygous108307850
1152112961152112962TG18GENIChomozygous108307854
1152115733152115734AG24GENIChomozygous108307856
1152116358152116359GA23GENIChomozygous108307858
1152116542152116543AG16GENIChomozygous108307860
1152120930152120931CT14GENIChomozygous108307862
1152121030152121031GA19GENIChomozygous108307864
1152121337152121338TC22GENIChomozygous109148519
1152121840152121841GA8GENIChomozygous108307866
1152128612152128613AG18GENIChomozygous108307872
1152130741152130742AG27GENIChomozygous108307874
1152131581152131582TC13GENIChomozygous108307876
1152132022152132023CT30GENIChomozygous108307878
1152132080152132081TC35GENIChomozygous108307880
1152132530152132531CT19GENIChomozygous108307882
1152136129152136130TC25GENIChomozygous108307888
1152136604152136605TC21GENIChomozygous108307890
1152136880152136881GC30GENIChomozygous108307892
1152140600152140601TG16GENIChomozygous108945369
1152143279152143280GA21GENIChomozygous108307898
1152143818152143819AG27GENIChomozygous108307900
1152144156152144157TC12GENIChomozygous108307902
1152145377152145378CA18GENIChomozygous108307904
1152146467152146468CT19GENIChomozygous108307906
1152147251152147252AG23GENIChomozygous108307908
1152147266152147267CT22GENIChomozygous108307910
1152150883152150884CT20GENIChomozygous108307912
1152152570152152571CT11GENIChomozygous108307916
1152152842152152843TC30GENIChomozygous108307918