| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128879404-128879669 | Common:4; Rare:129; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129183778-129184079 | Common:2; Rare:101 | ||||
| chr3:129249482-129249733 | Common:3; Rare:69 | ||||
| chr3:129439875-129440386 | Common:1; Rare:154; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129585919-129586254 | Common:1; Rare:126 | ||||
| chr3:129893567-129893891 | Rare:135 | ||||
| chr3:130746792-130746912 | Common:3; Rare:38 | ||||
| chr3:130893946-130894253 | Common:3; Rare:91 | ||||
| chr3:131026740-131026909 | Common:2; Rare:43 | ||||
| chr3:131381464-131381805 | Common:2; Rare:86 | ||||
| chr3:131502853-131502995 | Common:1; Rare:64 | ||||
| chr3:132659796-132659940 | Common:3; Rare:34 | ||||
| chr3:133661856-133662005 | Rare:34 | ||||
| chr3:134373717-134373824 | Rare:34 | ||||
| chr3:134374405-134374634 | Common:1; Rare:65 |