chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57833550878335509GA34GENIChomozygous113882988
57833569778335698AG33GENIChomozygous113882990
57833570578335706AG31GENIChomozygous113882992
57833603778336038AT28GENIChomozygous113882994
57833607478336075TC30GENIChomozygous113882996
57833618478336185CA40GENIChomozygous113882998
57833622378336224AG42GENIChomozygous113883000
57833649078336491TG34GENIChomozygous113883002
57833669478336695AG37GENIChomozygous113883004
57833674678336747GA40GENIChomozygous113883006
57833711778337118GA14GENIChomozygous113883008
57833818278338183AT27GENIChomozygous113883010
57833909478339095AG32GENIChomozygous113883012
57833991078339911GT28GENIChomozygous113883014
57834051378340514TC36GENIChomozygous113883016
57834058878340589CT17GENIChomozygous114127549
57834084378340844CT21GENIChomozygous113883018
57834271278342713CA24GENIChomozygous113883038
57834427478344275TC21GENICpossibly homozygous113883040
57834639078346391CA23GENIChomozygous113883042
57834729078347291AG22GENIChomozygous113883044
57835086178350862AC25GENIChomozygous113883046
57835120778351208CT25GENIChomozygous113883048
57835138478351385CT33GENIChomozygous113883050
57835238578352386CA13GENIChomozygous113883052
57835412678354127TC49GENIChomozygous113883054
57835441778354418AG31GENIChomozygous113883056
57835622778356228TC27GENIChomozygous113883058