| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:139389542-139389848 | Common:1; Rare:99 | ||||
| chr3:139390173-139390457 | Common:1; Rare:56 | ||||
| chr3:141231607-141231888 | Common:2; Rare:96 | ||||
| chr3:141402300-141402425 | Rare:37 | ||||
| chr3:143001453-143001631 | Common:2; Rare:64 | ||||
| chr3:146160958-146161386 | Common:2; Rare:131; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146163649-146163927 | Rare:47 | ||||
| chr3:146544545-146544681 | Common:3; Rare:26 | ||||
| chr3:148991392-148991620 | Common:2; Rare:105; Clinvar (benign):1 | ||||
| chr3:149377644-149377790 | Common:1; Rare:37 | ||||
| chr3:149657979-149658175 | Rare:41 | ||||
| chr3:149813004-149813265 | Common:2; Rare:86 | ||||
| chr3:150603149-150603395 | Common:2; Rare:98 | ||||
| chr3:150703714-150704036 | Common:3; Rare:164 | ||||
| chr3:152268587-152269133 | Common:2; Rare:200 |