| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:186503777-186503827 | Rare:6 | ||||
| chr2:188606036-188606160 | Rare:36 | ||||
| chr2:188969305-188969507 | Rare:29 | ||||
| chr2:188976683-188976875 | Common:1; Rare:34 | ||||
| chr2:188978716-188978872 | Common:3; Rare:26 | ||||
| chr2:188979451-188979526 | Rare:14 | ||||
| chr2:188984229-188984647 | Common:3; Rare:66 | ||||
| chr2:188988555-188988653 | Rare:34; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):11 | ||||
| chr2:188990092-188990396 | Rare:87; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):6 | ||||
| chr2:188990957-188991091 | Rare:44; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
| chr2:188992783-188992940 | Common:1; Rare:38; Clinvar (pathogenic):5 | ||||
| chr2:188993282-188993516 | Rare:43; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
| chr2:188993592-188993832 | Rare:31 | ||||
| chr2:188994015-188994349 | Common:2; Rare:92; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):7 | ||||
| chr2:188994510-188994613 | Rare:26; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):3 |