chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135104756351047564AACG20INTERGENICheterozygous50517700
135104756551047567CA--20INTERGENICheterozygous50517701
135105059951050600AACG23INTERGENIChomozygous49755760
135105314751053148T-11INTERGENIChomozygous49755765
135105889551058896AATG6INTERGENICheterozygous49755766
135105889551058896AATGTG6INTERGENICheterozygous49755767
135107046351070464C-7INTERGENICheterozygous50036440
135107222551072226G-23INTERGENIChomozygous49755769
135107224351072244C-25INTERGENIChomozygous49755770
135107225451072255CA28INTERGENIChomozygous49755771
135107226751072268AG30INTERGENIChomozygous49755772
135107228351072284AT23INTERGENIChomozygous49755773
135107240851072409AT28INTERGENIChomozygous49755774
135107241651072417CCA32INTERGENIChomozygous49755775
135107244351072444TTA32INTERGENIChomozygous49755776
135107244951072450TC33INTERGENIChomozygous49755777
135107245751072458GGA32INTERGENIChomozygous49755778
135107246451072465TTA34INTERGENIChomozygous49755779
135107246951072470AC33INTERGENIChomozygous49755780
135107500751075008GC18INTERGENIChomozygous49755781
135107503351075034AC17INTERGENIChomozygous49755782
135107564851075649TC21INTERGENIChomozygous49755783
135107606851076069GGCA10INTERGENIChomozygous49755784
135107568351075684TG21INTERGENIChomozygous49947064
135107568451075685GT21INTERGENIChomozygous49947065
135107013951070142GTG---9INTERGENICheterozygous50229929
135107564951075650CA20INTERGENIChomozygous50495113