| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65570276-65570504 | Rare:83 | ||||
| chr11:65572444-65572545 | Rare:30 | ||||
| chr11:65591852-65592282 | Common:4; Rare:216 | ||||
| chr11:65614054-65614423 | Rare:83 | ||||
| chr11:65615913-65616313 | Common:2; Rare:159 | ||||
| chr11:65637780-65638210 | Common:4; Rare:147 | ||||
| chr11:65662894-65663093 | Common:1; Rare:50 | ||||
| chr11:65663477-65663597 | Common:1; Rare:21 | ||||
| chr11:65711828-65712042 | Rare:66 | ||||
| chr11:65712501-65712631 | Common:2; Rare:50 | ||||
| chr11:65720360-65720798 | Common:2; Rare:314; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:65780790-65781180 | Common:3; Rare:125 | ||||
| chr11:65833802-65833990 | Rare:42 | ||||
| chr11:65858109-65858426 | Common:2; Rare:111 | ||||
| chr11:65859090-65859639 | Common:1; Rare:134 |