Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155967763-155967933 | Rare:38 | ||||
chr1:156038711-156039005 | Common:2; Rare:44 | ||||
chr1:156092415-156092589 | Rare:34 | ||||
chr1:156103233-156103296 | Rare:7 | ||||
chr1:156130298-156130772 | Common:3; Rare:115; Clinvar:11; Clinvar (benign):6; Clinvar (pathogenic):6 | ||||
chr1:156216358-156216438 | Common:2; Rare:9 | ||||
chr1:156223700-156223818 | Common:1; Rare:23 | ||||
chr1:156274188-156274537 | Common:3; Rare:50 | ||||
chr1:156279007-156279206 | Common:2; Rare:49 | ||||
chr1:156290388-156290490 | Common:2; Rare:13 | ||||
chr1:156317191-156317550 | Rare:87 | ||||
chr1:156497881-156498092 | Rare:45 | ||||
chr1:156498557-156498900 | Common:3; Rare:67 | ||||
chr1:156502891-156503091 | Common:1; Rare:37 | ||||
chr1:156503354-156503610 | Common:1; Rare:48 |