chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
61106784511067846CA63GENIChomozygous126411419
61107120311071204CA71GENIChomozygous118584810
61107476411074764T63GENIChomozygous128313944
61107477111074771A64GENIChomozygous128313945
61107485011074851C50GENIChomozygous128313946
61107496811074969TA63GENIChomozygous114723415
61107484411074845CA50GENIChomozygous114723408
61107488411074885TA53GENIChomozygous114723410
61107491411074915AT60GENIChomozygous114723412
61107492111074922TA60GENIChomozygous114723413
61107485111074852CA50GENIChomozygous118552310
61107500611075007TA61GENIChomozygous114723419
61107889911078900CT64GENIChomozygous114723427
61107934311079343C36GENIChomozygous128313947
61107934711079347C39GENIChomozygous128313948
61107935211079352C39GENIChomozygous128313949
61107935511079356CT42GENIChomozygous115044304
61107935711079358GC42GENIChomozygous115044305
61107940411079404A47GENIChomozygous129925058
61107940611079406G48GENIChomozygous129925059
61107942311079424CG45GENIChomozygous115044306
61107944611079446T42GENIChomozygous129925060
61107946411079464C40GENIChomozygous129925061
61107946811079468C41GENIChomozygous129925062
61107948111079481T45GENIChomozygous129925063
61107949311079494GA45GENIChomozygous114723429
61107951411079515G43GENIChomozygous129925064
61107953111079531CT36GENIChomozygous129925065
61107953911079539GG37GENIChomozygous129925066
61107954911079549T40GENIChomozygous129925067
61107956411079564C44GENIChomozygous129925068
61107957111079571C47GENIChomozygous129925069
61107957811079578T51GENIChomozygous129925070
61107958411079585C53GENIChomozygous129925071
61107958911079590G54GENIChomozygous129925072
61107959111079592G52GENIChomozygous129925073
61107959411079595G52GENIChomozygous129925074
61107942411079425GC45GENIChomozygous118598215