chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135104756351047564AACG20INTERGENICheterozygous50517700
135104756551047567CA--20INTERGENICheterozygous50517701
135105059951050600AACG23INTERGENIChomozygous49755760
135105314751053148T-7INTERGENIChomozygous49755765
135105982951059833AAGA----1INTERGENIChomozygous50617180
135106741251067420CTTTCTTT--------6INTERGENIChomozygous50605188
135106752451067528TTCT----18INTERGENIChomozygous50036421
135107222551072226G-13INTERGENIChomozygous49755769
135107224351072244C-6INTERGENIChomozygous49755770
135107225451072255CA7INTERGENIChomozygous49755771
135107226751072268AG8INTERGENIChomozygous49755772
135107228351072284AT13INTERGENIChomozygous49755773
135107240851072409AT18INTERGENIChomozygous49755774
135107241651072417CCA24INTERGENIChomozygous49755775
135107244351072444TTA16INTERGENIChomozygous49755776
135107244951072450TC16INTERGENIChomozygous49755777
135107245751072458GGA18INTERGENIChomozygous49755778
135107246451072465TTA19INTERGENIChomozygous49755779
135107246951072470AC18INTERGENIChomozygous49755780
135107500751075008GC18INTERGENIChomozygous49755781
135107503351075034AC23INTERGENIChomozygous49755782
135107564851075649TC21INTERGENIChomozygous49755783
135107564951075650CA23INTERGENIChomozygous50495113
135107606851076069GGCA6INTERGENIChomozygous49755784
135107568351075684TG22INTERGENIChomozygous49947064
135107568451075685GT22INTERGENIChomozygous49947065