chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117052068117052069AG17GENICheterozygous927912983
8117054122117054123CT17GENICheterozygous927912984
8117054158117054159AG19GENICheterozygous927912985
8117055685117055686CT6GENICheterozygous927912986
8117058726117058727CT32GENICheterozygous927912987
8117062340117062341TTGTCA40GENICheterozygous927945563
8117065011117065012AG34GENICheterozygous927912988
8117066348117066349CT17GENICheterozygous927912989
8117066426117066427GA24GENICheterozygous927912990
8117067190117067191GGCTGT27GENICheterozygous927945564
8117067250117067251AG36GENICheterozygous927912991
8117067587117067588TC18GENICheterozygous927912992
8117068680117068681CA23GENICheterozygous927912993
8117068800117068801AG33GENICheterozygous927912994
8117068936117068937TTTC20GENICheterozygous927945565
8117071534117071535CT14GENICheterozygous927912995
8117071896117071897GA16GENICheterozygous927912996
8117072006117072007CT18GENICheterozygous927912997
8117072252117072253AAG12GENICheterozygous927945566
8117072978117072979AG26GENICheterozygous927912998
8117074996117074997AG52GENICheterozygous927912999
8117075165117075166AG16GENICheterozygous927913000