| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141231652-141231888 | Common:2; Rare:83 | ||||
| chr3:141368495-141368540 | Rare:8 | ||||
| chr3:141386749-141386887 | Rare:15 | ||||
| chr3:142447968-142448110 | Common:1; Rare:50 | ||||
| chr3:143001472-143001647 | Common:2; Rare:65 | ||||
| chr3:146251000-146251233 | Common:2; Rare:57 | ||||
| chr3:146544514-146544876 | Common:4; Rare:86 | ||||
| chr3:149129545-149129711 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377515-149377816 | Common:1; Rare:82 | ||||
| chr3:149657934-149658200 | Rare:56 | ||||
| chr3:149812595-149812745 | Common:1; Rare:42 | ||||
| chr3:150603145-150603342 | Common:2; Rare:71 | ||||
| chr3:150703910-150704054 | Rare:44 | ||||
| chr3:151278364-151278469 | Common:1; Rare:19 | ||||
| chr3:152268557-152269287 | Common:2; Rare:249 |