chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57833550878335509GA15GENIChomozygous113882988
57833569778335698AG23GENIChomozygous113882990
57833570578335706AG25GENIChomozygous113882992
57833603778336038AT22GENIChomozygous113882994
57833607478336075TC26GENIChomozygous113882996
57833618478336185CA26GENIChomozygous113882998
57833622378336224AG25GENIChomozygous113883000
57833649078336491TG20GENIChomozygous113883002
57833669478336695AG31GENIChomozygous113883004
57833674678336747GA23GENICpossibly homozygous113883006
57833711778337118GA17GENIChomozygous113883008
57833818278338183AT34GENIChomozygous113883010
57833909478339095AG31GENIChomozygous113883012
57833991078339911GT42GENIChomozygous113883014
57834051378340514TC29GENIChomozygous113883016
57834084378340844CT16GENIChomozygous113883018
57834271278342713CA22GENIChomozygous113883038
57834427478344275TC22GENIChomozygous113883040
57834639078346391CA33GENIChomozygous113883042
57834729078347291AG17GENIChomozygous113883044
57835086178350862AC21GENIChomozygous113883046
57835120778351208CT21GENIChomozygous113883048
57835138478351385CT24GENIChomozygous113883050
57835238578352386CA23GENIChomozygous113883052
57835412678354127TC38GENIChomozygous113883054
57835441778354418AG26GENIChomozygous113883056
57835622778356228TC36GENIChomozygous113883058