chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117052068117052069AG15GENICheterozygous53222549
8117052890117052891AG10GENICheterozygous52829228
8117054122117054123CT20GENICheterozygous52829230
8117054158117054159AG15GENICheterozygous52829231
8117055685117055686CT16GENICheterozygous52829240
8117056327117056328CA40GENICheterozygous52829242
8117056459117056460GA37GENICheterozygous52829243
8117057218117057219T-50GENICheterozygous52829244
8117058388117058389AG25GENICheterozygous52829245
8117059204117059205AC50GENICheterozygous52829246
8117060807117060808CT17GENICheterozygous52829248
8117061256117061257CT33GENICheterozygous52829250
8117061986117061987CT11GENICheterozygous52829251
8117062340117062341TTGTCA61GENICheterozygous52829253
8117067007117067008CT26GENICheterozygous53612943
8117067190117067191GGCTGT30GENICheterozygous52829260
8117067250117067251AG33GENICheterozygous52829261
8117067587117067588TC23GENICheterozygous52829262
8117068376117068377TC33GENICheterozygous53612944
8117068426117068427CG34GENICheterozygous53612945
8117068510117068511AG27GENICheterozygous52829263
8117068680117068681CA32GENICheterozygous52829265
8117068800117068801AG25GENICheterozygous52829266
8117068936117068937TTTC19GENICheterozygous52829267
8117071137117071138GA11GENICheterozygous53612946
8117074996117074997AG26GENICheterozygous52829280