| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:143001472-143001631 | Common:2; Rare:57 | ||||
| chr3:143971975-143972077 | Common:1; Rare:40 | ||||
| chr3:146160963-146161279 | Common:1; Rare:106; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:146251010-146251148 | Common:1; Rare:33 | ||||
| chr3:146544471-146544930 | Common:5; Rare:112 | ||||
| chr3:149129549-149129687 | Common:1; Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149333408-149333521 | Common:3; Rare:20 | ||||
| chr3:149333573-149333636 | Rare:10 | ||||
| chr3:149377369-149377841 | Common:1; Rare:140 | ||||
| chr3:149657953-149658175 | Rare:46 | ||||
| chr3:150408090-150408311 | Common:1; Rare:75 | ||||
| chr3:150603145-150603372 | Common:2; Rare:87 | ||||
| chr3:150703900-150704025 | Rare:44 | ||||
| chr3:151873339-151873663 | Rare:39 | ||||
| chr3:152268594-152269386 | Common:2; Rare:267 |