chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3131011277131011278C-14GENIChomozygous57677912
3131011820131011821GC48GENIChomozygous57677914
3131013352131013353TC8GENIChomozygous57677916
3131013356131013357AC8GENIChomozygous57677918
3131014014131014015CA47GENIChomozygous57677920
3131014235131014239CAGA----28GENIChomozygous57677922
3131015291131015292GGTTATTTATTTAT1GENIChomozygous57677924
3131015451131015452TC36GENIChomozygous57677926
3131015572131015573TC54GENIChomozygous57677928
3131015791131015792CT43GENIChomozygous57677930
3131016350131016351AG35GENIChomozygous57677932
3131016678131016679CT11GENIChomozygous57677934
3131016835131016836TC41GENIChomozygous57677936
3131017390131017391AT47GENIChomozygous57677938
3131017701131017702AG40GENIChomozygous57677940
3131017787131017788GGCT32GENIChomozygous57677942
3131017845131017846CT21GENIChomozygous57677943
3131018010131018011T-28GENIChomozygous57677945
3131018182131018183CA48GENIChomozygous57677947
3131019069131019070AG30GENIChomozygous57677949
3131019094131019095CT29GENIChomozygous57677951
3131019275131019276GA44GENIChomozygous57677953
3131020111131020112TC46GENIChomozygous57677957
3131020178131020179AC33GENIChomozygous57677959
3131020198131020199GA31GENIChomozygous57677961
3131020240131020241CT29GENIChomozygous57677963
3131020592131020596TTTT----25GENIChomozygous57677965
3131021119131021123TTGA----31GENIChomozygous57677967
3131022283131022284C-18GENICpossibly homozygous57677969
3131022445131022446TC37GENIChomozygous57677971
3131022486131022487TC34GENIChomozygous57677973
3131022846131022851TGTGG-----15GENIChomozygous57677975
3131024554131024555AT45GENIChomozygous57677977
3131025138131025139GA34GENIChomozygous57677979