chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117644037117644038TC12GENIChomozygous115847861
7117644352117644353CT21GENIChomozygous115847863
7117644491117644492GA20GENIChomozygous115847865
7117645860117645861AG18GENIChomozygous115847867
7117647114117647115GA29GENIChomozygous115847869
7117647680117647681CT16GENIChomozygous115847871
7117647757117647758AG19GENIChomozygous115847873
7117647908117647909GA14GENIChomozygous115847875
7117648105117648106TC10GENIChomozygous115847877
7117649402117649403AC20GENIChomozygous115847879
7117650804117650805AT16GENIChomozygous115847881
7117650819117650820TA15GENIChomozygous115847883
7117654277117654278GC21GENIChomozygous115847885
7117654443117654444AG16GENIChomozygous115847887
7117655200117655201CG17GENIChomozygous116080608
7117655834117655835GA28GENIChomozygous115847889
7117655896117655897AT26GENIChomozygous115847891
7117658391117658392CT12GENIChomozygous115847893
7117660088117660089CA12GENIChomozygous115847895
7117660212117660213TC23GENIChomozygous115847897
7117660324117660325CT19GENIChomozygous115847899
7117660654117660655TG24GENIChomozygous115847901
7117661438117661439GA23GENIChomozygous115847903
7117661589117661590GA17GENIChomozygous115847905