| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128153339-128153499 | Common:1; Rare:43 | ||||
| chr3:128493200-128493292 | Rare:32 | ||||
| chr3:128650541-128650905 | Common:2; Rare:151 | ||||
| chr3:128725987-128726233 | Common:1; Rare:76; Clinvar:3 | ||||
| chr3:128879408-128879694 | Common:4; Rare:141; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129001218-129001370 | Common:1; Rare:39 | ||||
| chr3:129160981-129161122 | Rare:54 | ||||
| chr3:129183778-129184090 | Common:2; Rare:108 | ||||
| chr3:129249524-129249746 | Common:2; Rare:62 | ||||
| chr3:129278764-129278943 | Common:3; Rare:54 | ||||
| chr3:129316227-129316391 | Common:1; Rare:67 | ||||
| chr3:129439732-129440418 | Common:1; Rare:214; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:129488064-129488347 | Common:3; Rare:87; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:129560694-129560788 | Common:1; Rare:22 | ||||
| chr3:129893523-129893882 | Rare:137 |