| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65540641-65540850 | Common:3; Rare:84 | ||||
| chr11:65540986-65541079 | Common:1; Rare:18 | ||||
| chr11:65546639-65546892 | Common:2; Rare:75; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:65558188-65558490 | Common:3; Rare:65 | ||||
| chr11:65558598-65558732 | Common:3; Rare:23 | ||||
| chr11:65558926-65559048 | Rare:21 | ||||
| chr11:65559262-65559394 | Common:1; Rare:23 | ||||
| chr11:65569980-65570149 | Common:1; Rare:54 | ||||
| chr11:65570257-65570535 | Rare:106 | ||||
| chr11:65572444-65572645 | Rare:66 | ||||
| chr11:65572751-65572834 | Rare:14 | ||||
| chr11:65572902-65573190 | Rare:68 | ||||
| chr11:65606950-65607389 | Common:3; Rare:143 | ||||
| chr11:65607489-65607517 | Rare:7 | ||||
| chr11:65614186-65614561 | Rare:84 |