chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108204797682047977CA28GENIChomozygous116812518
108206223182062232GT31GENIChomozygous116812522
108207055882070559CT26GENIChomozygous116658028
108207426582074266AC11GENIChomozygous116658030
108207660282076603CT17GENIChomozygous116812524
108207743882077439AG18GENIChomozygous116658038
108207838282078383TC32GENIChomozygous116658040
108208114782081148TC25GENIChomozygous116658050
108208893982088940CT44GENIChomozygous116658058
108208894182088942CA45GENIChomozygous116658060
108208907682089077GA26GENIChomozygous116812526
108208928582089286TC26GENIChomozygous116658062
108209057082090571AT26GENIChomozygous116658064
108209233282092333CT19GENIChomozygous116812528
108209386682093867TA21GENIChomozygous116658066
108209415982094160GA16GENIChomozygous116658068
108209418182094182GA13GENIChomozygous116658070
108209474482094745TC24GENIChomozygous116658072
108209582882095829GA22GENIChomozygous116658074
108209607282096073TA30GENIChomozygous116812530
108209638582096386CT21GENIChomozygous116812532
108210325382103254TC22GENIChomozygous116658076
108210679782106798CA21GENIChomozygous116658078
108210687982106880TG34GENIChomozygous116658080
108210872282108723GA21GENIChomozygous116812534
108210939982109400AT14GENIChomozygous116658082
108210943082109431TC29GENIChomozygous116658084
108211446682114467TC26GENIChomozygous116658086