chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117052068117052069AG14GENICheterozygous925281831
8117052890117052891AG27GENICheterozygous925281832
8117054122117054123CT8GENICheterozygous925281833
8117054158117054159AG12GENICheterozygous925281834
8117055685117055686CT10GENICheterozygous925281835
8117058726117058727CT27GENICheterozygous925281836
8117062340117062341TTGTCA42GENICheterozygous925316071
8117065011117065012AG34GENICheterozygous925281837
8117067190117067191GGCTGT25GENICheterozygous925316072
8117067250117067251AG29GENICheterozygous925281838
8117067587117067588TC25GENICheterozygous925281839
8117068680117068681CA31GENICheterozygous925281840
8117068800117068801AG29GENICheterozygous925281841
8117068936117068937TTTC23GENICheterozygous925316073
8117071534117071535CT15GENICheterozygous925281842
8117071896117071897GA13GENICheterozygous925281843
8117072006117072007CT13GENICheterozygous925281844
8117072252117072253AAG16GENICheterozygous925316074
8117072978117072979AG29GENICheterozygous925281845
8117074996117074997AG29GENICheterozygous925281846