chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117052068117052069AG13GENICheterozygous925639838
8117052890117052891AG5GENICheterozygous925639839
8117054122117054123CT14GENICheterozygous925639840
8117054158117054159AG12GENICheterozygous925639841
8117055685117055686CT10GENICheterozygous925639842
8117058726117058727CT28GENICheterozygous925639843
8117062340117062341TTGTCA22GENICheterozygous925671462
8117065011117065012AG35GENICheterozygous925639844
8117066348117066349CT6GENICheterozygous925639845
8117067190117067191GGCTGT26GENICheterozygous925671463
8117067250117067251AG36GENICheterozygous925639846
8117067587117067588TC26GENICheterozygous925639847
8117068680117068681CA23GENICheterozygous925639848
8117068800117068801AG18GENICheterozygous925639849
8117068936117068937TTTC21GENICheterozygous925671464
8117071534117071535CT9GENICheterozygous925639850
8117071592117071593CA11GENICheterozygous925639851
8117071896117071897GA7GENICheterozygous925639852
8117072006117072007CT16GENICheterozygous925639853
8117072252117072253AAG10GENICheterozygous925671465
8117072978117072979AG13GENICheterozygous925639854
8117074996117074997AG24GENICheterozygous925639855
8117075165117075166AG6GENICheterozygous925639856