| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:146070771-146071110 | Common:1; Rare:75; Clinvar:1 | ||||
| chr3:146160890-146161017 | Rare:44; Clinvar (benign):1 | ||||
| chr3:146161019-146161214 | Common:1; Rare:68; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:146161309-146161450 | Common:2; Rare:30; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:147393119-147393442 | Common:1; Rare:85 | ||||
| chr3:149129458-149129714 | Common:3; Rare:111; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377617-149377950 | Common:1; Rare:65 | ||||
| chr3:149657995-149658273 | Rare:70 | ||||
| chr3:149970835-149971023 | Rare:93 | ||||
| chr3:149971102-149971276 | Common:4; Rare:65 | ||||
| chr3:150408471-150408643 | Rare:56 | ||||
| chr3:150603181-150603323 | Common:1; Rare:55 | ||||
| chr3:152268848-152269069 | Rare:77 | ||||
| chr3:152269509-152269703 | Rare:55 | ||||
| chr3:155079634-155080046 | Common:4; Rare:106 |