chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117052068117052069AG14GENICheterozygous926240224
8117052890117052891AG7GENICheterozygous926240225
8117054122117054123CT18GENICheterozygous926240226
8117054158117054159AG23GENICheterozygous926240227
8117055685117055686CT15GENICheterozygous926240228
8117058726117058727CT36GENICheterozygous926240229
8117062340117062341TTGTCA29GENICheterozygous926271547
8117065011117065012AG36GENICheterozygous926240230
8117065486117065487TA39GENICheterozygous926240231
8117066426117066427GA10GENICheterozygous926240232
8117067190117067191GGCTGT29GENICheterozygous926271548
8117067250117067251AG23GENICheterozygous926240233
8117067587117067588TC23GENICheterozygous926240234
8117068680117068681CA17GENICheterozygous926240235
8117068800117068801AG27GENICheterozygous926240236
8117068936117068937TTTC14GENICheterozygous926271549
8117071534117071535CT8GENICheterozygous926240237
8117071896117071897GA6GENICheterozygous926240238
8117072006117072007CT14GENICheterozygous926240239
8117072252117072253AAG8GENICheterozygous926271550
8117072978117072979AG8GENICheterozygous926240240
8117074996117074997AG33GENICheterozygous926240241
8117075165117075166AG9GENICheterozygous926240242