| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52705768-52706181 | Common:2; Rare:145 | ||||
| chr3:57597314-57597661 | Common:4; Rare:109 | ||||
| chr3:62318890-62319049 | Rare:67 | ||||
| chr3:67654590-67654799 | Common:2; Rare:77 | ||||
| chr3:88058967-88059308 | Common:2; Rare:124 | ||||
| chr3:101686672-101686860 | Common:2; Rare:81 | ||||
| chr3:122384043-122384258 | Rare:79 | ||||
| chr3:129440015-129440151 | Common:1; Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:131381464-131381786 | Common:2; Rare:80 | ||||
| chr3:134485976-134486045 | Common:2; Rare:27 | ||||
| chr3:139389617-139389857 | Common:1; Rare:75 | ||||
| chr3:149377644-149377831 | Common:1; Rare:45 | ||||
| chr3:149812992-149813260 | Common:2; Rare:87 | ||||
| chr3:150603173-150603355 | Common:2; Rare:72 | ||||
| chr3:156555052-156555335 | Common:1; Rare:117 |