| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:37861470-37862030 | Common:3; Rare:184 | ||||
| chr3:38136988-38137447 | Common:2; Rare:234 | ||||
| chr3:38164830-38165320 | Common:3; Rare:180 | ||||
| chr3:38165424-38165857 | Common:2; Rare:226 | ||||
| chr3:38346704-38346861 | Rare:48 | ||||
| chr3:38453673-38453922 | Rare:86 | ||||
| chr3:38496001-38496640 | Common:4; Rare:344 | ||||
| chr3:39051936-39052046 | Common:1; Rare:40 | ||||
| chr3:39052414-39052526 | Rare:36 | ||||
| chr3:39106820-39107300 | Common:13; Rare:281 | ||||
| chr3:39107539-39107732 | Common:6; Rare:96 | ||||
| chr3:39153537-39153796 | Common:7; Rare:163 | ||||
| chr3:39383272-39383456 | Common:4; Rare:62; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:39383530-39383651 | Rare:26; Clinvar:1 | ||||
| chr3:39406514-39406767 | Common:8; Rare:188 |