chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117052068117052069AG9GENICheterozygous925102226
8117052890117052891AG19GENICheterozygous925102227
8117054122117054123CT15GENICheterozygous925102228
8117054158117054159AG12GENICheterozygous925102229
8117055685117055686CT10GENICheterozygous925102230
8117058726117058727CT28GENICheterozygous925102231
8117062340117062341TTGTCA40GENICheterozygous925133798
8117065011117065012AG38GENICheterozygous925102232
8117067190117067191GGCTGT25GENICheterozygous925133799
8117067250117067251AG21GENICheterozygous925102233
8117067587117067588TC23GENICheterozygous925102234
8117068680117068681CA35GENICheterozygous925102235
8117068800117068801AG27GENICheterozygous925102236
8117068936117068937TTTC13GENICheterozygous925133800
8117071534117071535CT12GENICheterozygous925102237
8117072006117072007CT18GENICheterozygous925102238
8117072252117072253AAG12GENICheterozygous925133801
8117072978117072979AG13GENICheterozygous925102239
8117074996117074997AG33GENICheterozygous925102240
8117075165117075166AG14GENICheterozygous925102241