chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117052890117052891AG40GENICheterozygous926419056
8117054122117054123CT20GENICheterozygous926419057
8117054158117054159AG20GENICheterozygous926419058
8117055685117055686CT20GENICheterozygous926419059
8117056327117056328CA69GENICheterozygous926419060
8117056459117056460GA61GENICheterozygous926419061
8117057218117057219T-42GENICheterozygous926453168
8117058388117058389AG45GENICheterozygous926419062
8117059204117059205AC54GENICheterozygous926419063
8117060807117060808CT32GENICheterozygous926419064
8117061256117061257CT57GENICheterozygous926419065
8117061986117061987CT11GENICheterozygous926419066
8117062340117062341TTGTCA35GENICheterozygous926453169
8117062839117062840CG67GENICheterozygous926419067
8117067190117067191GGCTGT24GENICheterozygous926453170
8117067250117067251AG26GENICheterozygous926419068
8117067587117067588TC19GENICheterozygous926419069
8117068510117068511AG44GENICheterozygous926419070
8117068680117068681CA34GENICheterozygous926419071
8117068800117068801AG36GENICheterozygous926419072
8117068936117068937TTTC14GENICheterozygous926453171
8117074996117074997AG38GENICheterozygous926419073