chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117052068117052069AG27GENICheterozygous926791876
8117052890117052891AG17GENICheterozygous926791877
8117054122117054123CT11GENICheterozygous926791878
8117054158117054159AG16GENICheterozygous926791879
8117055685117055686CT11GENICheterozygous926791880
8117058726117058727CT34GENICheterozygous926791881
8117062340117062341TTGTCA49GENICheterozygous926823266
8117065011117065012AG32GENICheterozygous926791882
8117066348117066349CT5GENICheterozygous926791883
8117066426117066427GA9GENICheterozygous926791884
8117067190117067191GGCTGT20GENICheterozygous926823267
8117067250117067251AG19GENICheterozygous926791885
8117067587117067588TC31GENICheterozygous926791886
8117068680117068681CA49GENICheterozygous926791887
8117068800117068801AG34GENICheterozygous926791888
8117068936117068937TTTC11GENICheterozygous926823268
8117071534117071535CT13GENICheterozygous926791889
8117071896117071897GA8GENICheterozygous926791890
8117072006117072007CT16GENICheterozygous926791891
8117072252117072253AAG15GENICheterozygous926823269
8117072978117072979AG13GENICheterozygous926791892
8117074996117074997AG24GENICheterozygous926791893
8117075165117075166AG5GENICheterozygous926791894