| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129418434-129418585 | Common:2; Rare:69 | ||||
| chr3:129439829-129440368 | Common:1; Rare:243; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129606572-129607030 | Common:4; Rare:116 | ||||
| chr3:129656696-129656829 | Rare:49 | ||||
| chr3:129893523-129893906 | Rare:283 | ||||
| chr3:130746751-130746972 | Common:6; Rare:116 | ||||
| chr3:130893884-130894248 | Common:6; Rare:210 | ||||
| chr3:131026734-131026940 | Common:4; Rare:100 | ||||
| chr3:131381404-131381831 | Common:6; Rare:219 | ||||
| chr3:131502756-131503065 | Common:2; Rare:231 | ||||
| chr3:132659310-132659570 | Rare:79 | ||||
| chr3:132659742-132659999 | Common:6; Rare:115 | ||||
| chr3:133573230-133573760 | Common:12; Rare:221 | ||||
| chr3:133573841-133574064 | Rare:100 | ||||
| chr3:133574200-133574630 | Common:8; Rare:239 |