chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57833540878335409AG25GENIChomozygous119169207
57833550878335509GA27GENIChomozygous113882988
57833569778335698AG25GENIChomozygous113882990
57833570578335706AG25GENIChomozygous113882992
57833603778336038AT37GENIChomozygous113882994
57833607478336075TC36GENIChomozygous113882996
57833618478336185CA33GENIChomozygous113882998
57833622378336224AG26GENIChomozygous113883000
57833649078336491TG33GENIChomozygous113883002
57833659778336598CT27GENIChomozygous119169209
57833669478336695AG20GENIChomozygous113883004
57833731578337316GC39GENIChomozygous119169211
57833762378337624GA34GENIChomozygous119169213
57833818278338183AT32GENIChomozygous113883010
57833991078339911GT29GENIChomozygous113883014
57834051378340514TC21GENIChomozygous113883016
57834729078347291AG35GENIChomozygous113883044
57834909278349093CA29GENIChomozygous119169215
57835120578351206CT25GENIChomozygous119169217
57835138478351385CT27GENIChomozygous113883050
57835238578352386CA17GENIChomozygous113883052
57835388278353883CT20GENIChomozygous119203586
57835412678354127TC23GENIChomozygous113883054
57835422378354224CT32GENIChomozygous119169219
57835436978354370CA29GENIChomozygous119169221
57835441778354418AG30GENIChomozygous113883056
57835590678355907AT29GENIChomozygous119169223
57835622778356228TC27GENIChomozygous113883058