chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1835657873565788CG56GENIChomozygous110241951
1835662753566276CG58GENIChomozygous110241953
1835663353566336CT70GENIChomozygous110241956
1835668313566832TG67GENICpossibly homozygous110241958
1835666523566652CCCCT53GENIChomozygous129506041
1835721333572134TC65GENIChomozygous110241960
1835725063572507AG71GENIChomozygous110241962
1835750533575053T62GENICpossibly homozygous129506042
1835785653578566CT62GENICpossibly homozygous110241964
1835795903579591CT65GENIChomozygous110241966
1835826383582639CT55GENIChomozygous110241968
1835826613582666TGCTA50GENIChomozygous129506043
1835837023583703CT49GENIChomozygous110241970
1835853953585396GA73GENIChomozygous110241973
1835854453585446T79GENIChomozygous129506044
1835854473585449CT80GENIChomozygous129506045
1835897833589784TG55GENIChomozygous110241975
1835898503589851GA56GENIChomozygous110241977