| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128123565-128124167 | Rare:175 | ||||
| chr3:128153350-128153510 | Rare:47 | ||||
| chr3:128487899-128488064 | Common:1; Rare:43 | ||||
| chr3:128488511-128488630 | Common:1; Rare:28 | ||||
| chr3:128650546-128650608 | Rare:20 | ||||
| chr3:128650729-128650907 | Common:2; Rare:83 | ||||
| chr3:128680631-128680897 | Common:3; Rare:84 | ||||
| chr3:128725954-128726225 | Common:1; Rare:76; Clinvar:3 | ||||
| chr3:128879357-128879675 | Common:5; Rare:148; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129160971-129161477 | Common:2; Rare:157 | ||||
| chr3:129183778-129184123 | Common:2; Rare:130 | ||||
| chr3:129249524-129249707 | Common:2; Rare:55 | ||||
| chr3:129278762-129278895 | Common:4; Rare:43 | ||||
| chr3:129316276-129316338 | Rare:27 | ||||
| chr3:129439819-129440393 | Common:1; Rare:175; Clinvar:3; Clinvar (benign):1 |