| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:144520111-144520524 | Common:4; Rare:75; Clinvar (benign):1 | ||||
| chr2:148020692-148021279 | Common:2; Rare:139; Clinvar (benign):2 | ||||
| chr2:148021357-148021671 | Rare:79 | ||||
| chr2:148644601-148644751 | Rare:57 | ||||
| chr2:149587320-149587407 | Rare:17 | ||||
| chr2:149587681-149587905 | Common:1; Rare:67; Clinvar:1 | ||||
| chr2:150485382-150485495 | Rare:27 | ||||
| chr2:151828372-151828619 | Common:3; Rare:72 | ||||
| chr2:152717829-152717958 | Rare:53 | ||||
| chr2:152717982-152718296 | Common:1; Rare:103 | ||||
| chr2:152718485-152718654 | Rare:69 | ||||
| chr2:153478656-153478913 | Common:2; Rare:72 | ||||
| chr2:156332703-156332870 | Rare:49; Clinvar:2 | ||||
| chr2:156436041-156436410 | Common:3; Rare:105 | ||||
| chr2:157628733-157628920 | Rare:55 |