| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:151384745-151385060 | Common:1; Rare:67 | ||||
| chr3:152268585-152269311 | Common:2; Rare:244 | ||||
| chr3:152269544-152269712 | Rare:45 | ||||
| chr3:152298753-152299050 | Rare:56 | ||||
| chr3:154121264-154121457 | Common:3; Rare:83 | ||||
| chr3:155079003-155079159 | Rare:27 | ||||
| chr3:155079756-155080464 | Common:3; Rare:170 | ||||
| chr3:155083345-155083547 | Common:1; Rare:44 | ||||
| chr3:155854364-155854804 | Rare:127 | ||||
| chr3:155870323-155870741 | Common:2; Rare:119 | ||||
| chr3:156674333-156674618 | Common:4; Rare:83 | ||||
| chr3:156826115-156826364 | Common:3; Rare:78 | ||||
| chr3:157159945-157160295 | Rare:144 | ||||
| chr3:158651962-158652112 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:158672481-158672721 | Common:2; Rare:69 |