| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62601215-62601310 | Rare:23 | ||||
| chr11:62611542-62611841 | Rare:75 | ||||
| chr11:62612528-62612679 | Common:4; Rare:37 | ||||
| chr11:62612715-62612881 | Common:1; Rare:54; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:62626065-62626360 | Rare:81 | ||||
| chr11:62646562-62646883 | Common:2; Rare:123; Clinvar (pathogenic):1 | ||||
| chr11:62653250-62653413 | Common:1; Rare:58 | ||||
| chr11:62665143-62665327 | Common:4; Rare:85 | ||||
| chr11:62665434-62665672 | Common:2; Rare:91 | ||||
| chr11:62678857-62679174 | Rare:106 | ||||
| chr11:62706223-62706437 | Common:3; Rare:94; Clinvar (benign):5 | ||||
| chr11:62723592-62723960 | Common:1; Rare:100 | ||||
| chr11:62726619-62727118 | Common:1; Rare:202 | ||||
| chr11:62727127-62727535 | Common:2; Rare:186 | ||||
| chr11:62727540-62727640 | Rare:40 |