| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:142877511-142877664 | Common:1; Rare:24 | ||||
| chr2:144517341-144517579 | Rare:69; Clinvar:1; Clinvar (benign):4 | ||||
| chr2:148020673-148021109 | Common:2; Rare:101; Clinvar (benign):2 | ||||
| chr2:148021571-148021652 | Rare:17 | ||||
| chr2:149587310-149587390 | Rare:15 | ||||
| chr2:149587690-149587704 | Rare:5 | ||||
| chr2:151828446-151828793 | Common:2; Rare:96 | ||||
| chr2:152717829-152717942 | Rare:47 | ||||
| chr2:152717995-152718079 | Rare:25 | ||||
| chr2:152718491-152718654 | Rare:65 | ||||
| chr2:156436118-156436459 | Common:3; Rare:99 | ||||
| chr2:158968476-158968702 | Rare:72 | ||||
| chr2:159712390-159712583 | Common:2; Rare:79 | ||||
| chr2:160493412-160493569 | Common:1; Rare:46 | ||||
| chr2:162073464-162073564 | Common:1; Rare:40 |