| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141876470-141876682 | Common:1; Rare:82 | ||||
| chr3:141921731-141922060 | Common:1; Rare:58 | ||||
| chr3:142888817-142889258 | Common:4; Rare:100 | ||||
| chr3:143001472-143001646 | Common:2; Rare:64 | ||||
| chr3:146160973-146161386 | Common:2; Rare:127; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146250958-146251229 | Common:1; Rare:65 | ||||
| chr3:146544484-146544865 | Common:5; Rare:90 | ||||
| chr3:147392316-147392473 | Rare:45 | ||||
| chr3:147393360-147393503 | Common:1; Rare:43 | ||||
| chr3:149129549-149129692 | Common:1; Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377628-149377832 | Common:1; Rare:48 | ||||
| chr3:149657982-149658159 | Rare:37 | ||||
| chr3:149812672-149812779 | Common:1; Rare:34 | ||||
| chr3:149812958-149813337 | Common:2; Rare:119 | ||||
| chr3:149813741-149813855 | Rare:17 |