chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117052068117052069AG16GENICheterozygous925846181
8117052890117052891AG15GENICheterozygous925846182
8117054122117054123CT14GENICheterozygous925846183
8117054158117054159AG13GENICheterozygous925846184
8117055685117055686CT10GENICheterozygous925846185
8117058726117058727CT41GENICheterozygous925846186
8117062340117062341TTGTCA52GENICheterozygous925880061
8117065011117065012AG35GENICheterozygous925846187
8117066348117066349CT7GENICheterozygous925846188
8117066426117066427GA10GENICheterozygous925846189
8117067190117067191GGCTGT19GENICheterozygous925880062
8117067250117067251AG16GENICheterozygous925846190
8117067587117067588TC26GENICheterozygous925846191
8117068680117068681CA32GENICheterozygous925846192
8117068800117068801AG50GENICheterozygous925846193
8117068936117068937TTTC21GENICheterozygous925880063
8117071534117071535CT14GENICheterozygous925846194
8117071896117071897GA6GENICheterozygous925846195
8117072006117072007CT18GENICheterozygous925846196
8117072252117072253AAG10GENICheterozygous925880064
8117072978117072979AG19GENICheterozygous925846197
8117074996117074997AG26GENICheterozygous925846198
8117075165117075166AG7GENICheterozygous925846199