| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:148021483-148021671 | Rare:46 | ||||
| chr2:149587321-149587370 | Rare:10 | ||||
| chr2:149587664-149587683 | Rare:9; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:149587685-149587822 | Common:1; Rare:39; Clinvar:1 | ||||
| chr2:150485357-150485469 | Common:1; Rare:27 | ||||
| chr2:151828446-151828793 | Common:2; Rare:96 | ||||
| chr2:152717829-152717967 | Rare:59 | ||||
| chr2:152717991-152718149 | Common:1; Rare:45 | ||||
| chr2:152718481-152718643 | Rare:63 | ||||
| chr2:153478734-153479044 | Common:1; Rare:74 | ||||
| chr2:156332710-156332870 | Rare:48; Clinvar:2 | ||||
| chr2:156436084-156436468 | Common:3; Rare:105 | ||||
| chr2:159286638-159286900 | Common:5; Rare:99 | ||||
| chr2:159615225-159615344 | Common:2; Rare:28 | ||||
| chr2:159615453-159615724 | Common:2; Rare:89 |