| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129260270-129260400 | Rare:44 | ||||
| chr3:129278761-129278900 | Common:4; Rare:43 | ||||
| chr3:129316254-129316398 | Common:1; Rare:48 | ||||
| chr3:129439847-129440254 | Common:1; Rare:120; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:129893539-129893875 | Rare:132 | ||||
| chr3:130746796-130746929 | Common:3; Rare:40 | ||||
| chr3:130893919-130894237 | Common:3; Rare:91 | ||||
| chr3:131026729-131026955 | Common:2; Rare:57 | ||||
| chr3:131381441-131381849 | Common:3; Rare:115 | ||||
| chr3:131502747-131503023 | Common:1; Rare:110 | ||||
| chr3:132659756-132659980 | Common:3; Rare:53 | ||||
| chr3:132722144-132722210 | Common:1; Rare:33; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:133573837-133573994 | Rare:47 | ||||
| chr3:133661856-133662021 | Rare:38 | ||||
| chr3:134485386-134485877 | Common:1; Rare:121 |