chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117052890117052891AG12GENICheterozygous927381368
8117054122117054123CT18GENICheterozygous927381369
8117054158117054159AG24GENICheterozygous927381370
8117055685117055686CT14GENICheterozygous927381371
8117056327117056328CA46GENICheterozygous927381372
8117056459117056460GA36GENICheterozygous927381373
8117057218117057219T-34GENICheterozygous927416847
8117058388117058389AG21GENICheterozygous927381374
8117059204117059205AC42GENICheterozygous927381375
8117060807117060808CT33GENICheterozygous927381376
8117061256117061257CT21GENICheterozygous927381377
8117061986117061987CT21GENICheterozygous927381378
8117062340117062341TTGTCA56GENICheterozygous927416848
8117062839117062840CG60GENICheterozygous927381379
8117067190117067191GGCTGT15GENICheterozygous927416849
8117067250117067251AG10GENICheterozygous927381380
8117067587117067588TC19GENICheterozygous927381381
8117068510117068511AG28GENICheterozygous927381382
8117068680117068681CA23GENICheterozygous927381383
8117068800117068801AG36GENICheterozygous927381384
8117068936117068937TTTC21GENICheterozygous927416850
8117074996117074997AG20GENICheterozygous927381385