chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117052068117052069AG15GENICheterozygous927737551
8117052890117052891AG10GENICheterozygous927737552
8117054122117054123CT20GENICheterozygous927737553
8117054158117054159AG15GENICheterozygous927737554
8117055685117055686CT16GENICheterozygous927737555
8117056327117056328CA40GENICheterozygous927737556
8117056459117056460GA37GENICheterozygous927737557
8117057218117057219T-50GENICheterozygous927770331
8117058388117058389AG25GENICheterozygous927737558
8117059204117059205AC50GENICheterozygous927737559
8117060807117060808CT17GENICheterozygous927737560
8117061256117061257CT33GENICheterozygous927737561
8117061986117061987CT11GENICheterozygous927737562
8117062340117062341TTGTCA61GENICheterozygous927770332
8117067007117067008CT26GENICheterozygous927737563
8117067190117067191GGCTGT30GENICheterozygous927770333
8117067250117067251AG33GENICheterozygous927737564
8117067587117067588TC23GENICheterozygous927737565
8117068376117068377TC33GENICheterozygous927737566
8117068426117068427CG34GENICheterozygous927737567
8117068510117068511AG27GENICheterozygous927737568
8117068680117068681CA32GENICheterozygous927737569
8117068800117068801AG25GENICheterozygous927737570
8117068936117068937TTTC19GENICheterozygous927770334
8117071137117071138GA11GENICheterozygous927737571
8117074996117074997AG26GENICheterozygous927737572