chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117052068117052069AG14GENICheterozygous925462831
8117052890117052891AG28GENICheterozygous925462832
8117054122117054123CT16GENICheterozygous925462833
8117054158117054159AG13GENICheterozygous925462834
8117055685117055686CT12GENICheterozygous925462835
8117058726117058727CT77GENICheterozygous925462836
8117062340117062341TTGTCA55GENICheterozygous925494839
8117065011117065012AG32GENICheterozygous925462837
8117066348117066349CT15GENICheterozygous925462838
8117066426117066427GA8GENICheterozygous925462839
8117067190117067191GGCTGT29GENICheterozygous925494840
8117067250117067251AG24GENICheterozygous925462840
8117067587117067588TC33GENICheterozygous925462841
8117068680117068681CA42GENICheterozygous925462842
8117068800117068801AG30GENICheterozygous925462843
8117068936117068937TTTC28GENICheterozygous925494841
8117071534117071535CT15GENICheterozygous925462844
8117071896117071897GA18GENICheterozygous925462845
8117072006117072007CT16GENICheterozygous925462846
8117072252117072253AAG10GENICheterozygous925494842
8117072978117072979AG23GENICheterozygous925462847
8117074996117074997AG38GENICheterozygous925462848
8117075165117075166AG15GENICheterozygous925462849