| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141486857-141487074 | Common:1; Rare:67 | ||||
| chr3:142447968-142448130 | Common:1; Rare:57 | ||||
| chr3:142596293-142596418 | Common:1; Rare:32 | ||||
| chr3:143001436-143001661 | Common:3; Rare:87 | ||||
| chr3:146160961-146161386 | Common:2; Rare:129; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146163660-146163918 | Rare:43 | ||||
| chr3:146250977-146251272 | Common:2; Rare:72 | ||||
| chr3:146544536-146544824 | Common:4; Rare:68 | ||||
| chr3:149129545-149129701 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377369-149377832 | Common:1; Rare:138 | ||||
| chr3:149657982-149658200 | Rare:47 | ||||
| chr3:149813067-149813265 | Common:1; Rare:67 | ||||
| chr3:150603168-150603426 | Common:2; Rare:108 | ||||
| chr3:152268717-152269332 | Rare:203 | ||||
| chr3:152269533-152269689 | Rare:41 |