chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191073656310736564AG17GENIChomozygous109634852
191073674210736743GA17GENIChomozygous109634854
191073875210738753TG12GENIChomozygous109634858
191073877310738774TC14GENIChomozygous109634860
191073962610739627CT10GENIChomozygous109634862
191073963110739632TG11GENIChomozygous109634864
191073966110739662AG14GENIChomozygous109634866
191073987210739873TC10GENICheterozygous119596381
191073996310739964CT17GENIChomozygous109634868
191074058710740588TC17GENIChomozygous109634870
191074087710740878CT26GENIChomozygous109634872
191074257710742578GA25GENIChomozygous109634874
191074276510742766TG15GENIChomozygous109634876
191074460010744601GA25GENIChomozygous109634878
191074633210746333AG17GENIChomozygous109634880
191074738910747390GA26GENIChomozygous109634882
191074802310748024AG21GENIChomozygous109634884
191074960110749602CA22GENIChomozygous109634886
191075257110752572GA23GENIChomozygous109634888
191075142510751426TG4GENICheterozygous125262560
191074866110748662AT20GENICpossibly homozygous109764656