chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117644037117644038TC31GENIChomozygous115847861
7117644352117644353CT27GENIChomozygous115847863
7117644491117644492GA54GENICpossibly homozygous115847865
7117645860117645861AG32GENIChomozygous115847867
7117647114117647115GA82GENIChomozygous115847869
7117647680117647681CT55GENIChomozygous115847871
7117647757117647758AG66GENIChomozygous115847873
7117647908117647909GA56GENIChomozygous115847875
7117648105117648106TC43GENIChomozygous115847877
7117649402117649403AC41GENICpossibly homozygous115847879
7117650804117650805AT47GENIChomozygous115847881
7117650819117650820TA46GENIChomozygous115847883
7117654277117654278GC58GENIChomozygous115847885
7117654443117654444AG32GENIChomozygous115847887
7117655834117655835GA43GENIChomozygous115847889
7117655896117655897AT46GENIChomozygous115847891
7117658391117658392CT50GENIChomozygous115847893
7117660088117660089CA22GENIChomozygous115847895
7117660212117660213TC45GENIChomozygous115847897
7117660324117660325CT44GENICpossibly homozygous115847899
7117660654117660655TG56GENIChomozygous115847901
7117661438117661439GA54GENIChomozygous115847903
7117661589117661590GA50GENICpossibly homozygous115847905