chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1152073714152073715AG7GENIChomozygous108307786
1152076632152076633AG7GENIChomozygous108307788
1152077327152077328CT3GENIChomozygous108307790
1152079462152079463AG9GENIChomozygous108307792
1152080496152080497GC7GENICheterozygous120911374
1152082924152082925GA3GENIChomozygous108307794
1152084629152084630CT2GENIChomozygous108307796
1152084660152084661CT4GENIChomozygous108307798
1152085385152085386TC4GENIChomozygous108307800
1152091643152091644GA6GENIChomozygous108307802
1152098135152098136AC3GENIChomozygous108307826
1152098305152098306AT5GENIChomozygous108307828
1152107652152107653CT4GENIChomozygous108307850
1152110479152110480TG3GENIChomozygous108307852
1152112961152112962TG2GENIChomozygous108307854
1152115733152115734AG2GENIChomozygous108307856
1152116358152116359GA4GENIChomozygous108307858
1152116542152116543AG4GENIChomozygous108307860
1152121030152121031GA6GENIChomozygous108307864
1152121840152121841GA8GENIChomozygous108307866
1152125004152125005TA5GENICheterozygous120911375
1152125012152125013AG5GENICheterozygous120911376
1152128612152128613AG8GENIChomozygous108307872
1152130741152130742AG7GENIChomozygous108307874
1152131581152131582TC3GENIChomozygous108307876
1152132022152132023CT3GENIChomozygous108307878
1152132080152132081TC2GENIChomozygous108307880
1152132530152132531CT6GENIChomozygous108307882
1152136129152136130TC6GENIChomozygous108307888
1152136604152136605TC3GENIChomozygous108307890
1152142005152142006AG7GENIChomozygous108307894
1152143279152143280GA7GENIChomozygous108307898
1152143818152143819AG2GENIChomozygous108307900
1152146467152146468CT3GENIChomozygous108307906
1152147251152147252AG7GENIChomozygous108307908
1152147266152147267CT6GENIChomozygous108307910
1152150883152150884CT4GENIChomozygous108307912
1152152219152152220TG5GENIChomozygous108307914
1152152285152152286CT3GENIChomozygous109148521
1152152570152152571CT5GENIChomozygous108307916
1152152842152152843TC6GENIChomozygous108307918