chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117052890117052891AG32GENICheterozygous927187565
8117054122117054123CT10GENICheterozygous927187566
8117054158117054159AG16GENICheterozygous927187567
8117055685117055686CT17GENICheterozygous927187568
8117056327117056328CA56GENICheterozygous927187569
8117056459117056460GA70GENICheterozygous927187570
8117057218117057219T-61GENICheterozygous927229703
8117058388117058389AG46GENICheterozygous927187571
8117059204117059205AC51GENICheterozygous927187572
8117060807117060808CT32GENICheterozygous927187573
8117061256117061257CT39GENICheterozygous927187574
8117061986117061987CT13GENICheterozygous927187575
8117062340117062341TTGTCA52GENICheterozygous927229704
8117067190117067191GGCTGT26GENICheterozygous927229705
8117067250117067251AG32GENICheterozygous927187576
8117067587117067588TC27GENICheterozygous927187577
8117068376117068377TC29GENICheterozygous927187578
8117068426117068427CG40GENICheterozygous927187579
8117068510117068511AG46GENICheterozygous927187580
8117068680117068681CA53GENICheterozygous927187581
8117068800117068801AG36GENICheterozygous927187582
8117068936117068937TTTC21GENICheterozygous927229706
8117074996117074997AG33GENICheterozygous927187583