| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:229625944-229626219 | Rare:75 | ||||
| chr1:230714108-230714308 | Common:3; Rare:42; Clinvar:5; Clinvar (benign):3 | ||||
| chr1:231241122-231241362 | Common:2; Rare:114; Clinvar:4; Clinvar (benign):2 | ||||
| chr1:231337824-231338061 | Common:2; Rare:84 | ||||
| chr1:231528546-231528722 | Common:2; Rare:66 | ||||
| chr1:232805295-232805438 | Common:2; Rare:81 | ||||
| chr1:232950461-232950640 | Common:2; Rare:64 | ||||
| chr1:233613918-233614159 | Common:5; Rare:69 | ||||
| chr1:234373391-234373554 | Common:1; Rare:84; Clinvar (benign):3 | ||||
| chr1:235128772-235129025 | Rare:99 | ||||
| chr1:235328121-235328409 | Common:2; Rare:83 | ||||
| chr1:235328485-235328579 | Common:1; Rare:27 | ||||
| chr1:235328828-235329036 | Common:1; Rare:66 | ||||
| chr1:235866858-235867142 | Common:3; Rare:87 | ||||
| chr1:236065039-236065367 | Common:3; Rare:123; Clinvar (pathogenic):1 |