| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:37176222-37176458 | Common:1; Rare:135 | ||||
| chr3:37243143-37243460 | Common:2; Rare:151 | ||||
| chr3:37243610-37243980 | Common:4; Rare:187 | ||||
| chr3:37861703-37862015 | Common:2; Rare:129 | ||||
| chr3:37862086-37862225 | Rare:83 | ||||
| chr3:38024469-38024689 | Common:2; Rare:152 | ||||
| chr3:38133520-38133810 | Rare:74 | ||||
| chr3:38136982-38137447 | Common:2; Rare:237 | ||||
| chr3:38138473-38138715 | Common:4; Rare:135; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr3:38164850-38165330 | Common:3; Rare:205 | ||||
| chr3:38165434-38165684 | Common:2; Rare:162 | ||||
| chr3:38453701-38453975 | Common:1; Rare:85 | ||||
| chr3:39051917-39052045 | Common:2; Rare:79 | ||||
| chr3:39052170-39052610 | Common:4; Rare:237 | ||||
| chr3:39107547-39107717 | Common:5; Rare:96 |