| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129315865-129316065 | Common:1; Rare:45 | ||||
| chr3:129316233-129316379 | Common:1; Rare:62 | ||||
| chr3:129439846-129440382 | Common:1; Rare:161; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129893373-129893469 | Rare:27 | ||||
| chr3:129893539-129893896 | Rare:140 | ||||
| chr3:129974551-129974819 | Common:2; Rare:65 | ||||
| chr3:130746792-130746927 | Common:3; Rare:41 | ||||
| chr3:130893899-130894263 | Common:3; Rare:108 | ||||
| chr3:131026727-131026942 | Common:2; Rare:55 | ||||
| chr3:131381472-131381832 | Common:2; Rare:99 | ||||
| chr3:131502789-131503053 | Common:1; Rare:104 | ||||
| chr3:132317314-132317534 | Rare:51 | ||||
| chr3:132417148-132417736 | Common:6; Rare:195 | ||||
| chr3:132659779-132659983 | Common:3; Rare:46 | ||||
| chr3:133573859-133574017 | Rare:55 |