| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:110567290-110567804 | Common:8; Rare:336; Clinvar:4; Clinvar (benign):10 | ||||
| chr10:110871683-110872053 | Rare:198 | ||||
| chr10:110872237-110872574 | Rare:149 | ||||
| chr10:110918470-110918780 | Common:6; Rare:162 | ||||
| chr10:110919138-110919314 | Common:1; Rare:44 | ||||
| chr10:110919326-110919647 | Common:13; Rare:159; Clinvar:1 | ||||
| chr10:112183701-112183886 | Common:6; Rare:124 | ||||
| chr10:112375923-112376286 | Rare:114 | ||||
| chr10:112446738-112447365 | Common:6; Rare:254 | ||||
| chr10:112447490-112447750 | Common:3; Rare:106 | ||||
| chr10:112949970-112950410 | Common:6; Rare:172 | ||||
| chr10:113679778-113679938 | Common:4; Rare:118 | ||||
| chr10:113854319-113854898 | Common:1; Rare:210 | ||||
| chr10:114043600-114043910 | Common:2; Rare:94 | ||||
| chr10:114174146-114174407 | Rare:99 |