| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128052126-128052571 | Common:4; Rare:146 | ||||
| chr3:128123767-128124042 | Rare:71 | ||||
| chr3:128153350-128153510 | Rare:47 | ||||
| chr3:128650749-128650936 | Common:2; Rare:78 | ||||
| chr3:128680677-128681243 | Common:4; Rare:163 | ||||
| chr3:128725954-128726225 | Common:1; Rare:76; Clinvar:3 | ||||
| chr3:128726332-128726617 | Common:2; Rare:72; Clinvar (benign):2 | ||||
| chr3:128879380-128879692 | Common:5; Rare:150; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:129160996-129161477 | Common:2; Rare:151 | ||||
| chr3:129183805-129184117 | Common:2; Rare:116 | ||||
| chr3:129249512-129249707 | Common:2; Rare:58 | ||||
| chr3:129278733-129278895 | Common:4; Rare:49 | ||||
| chr3:129316238-129316325 | Rare:48 | ||||
| chr3:129439847-129440423 | Common:2; Rare:183; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:129893517-129893875 | Rare:137 |