| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18322521-18322626 | Common:1; Rare:48 | ||||
| chr11:18526885-18526980 | Rare:42 | ||||
| chr11:18588667-18588905 | Common:2; Rare:81 | ||||
| chr11:18634336-18634574 | Common:2; Rare:76 | ||||
| chr11:20363683-20363753 | Rare:17 | ||||
| chr11:20364117-20364240 | Rare:36 | ||||
| chr11:20387417-20387774 | Common:7; Rare:116 | ||||
| chr11:22625522-22625609 | Rare:43; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625808-22626011 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:27506729-27506861 | Common:1; Rare:61 | ||||
| chr11:28108130-28108416 | Common:1; Rare:84 | ||||
| chr11:31369735-31369876 | Rare:45 | ||||
| chr11:31509567-31509787 | Common:1; Rare:67 | ||||
| chr11:33039727-33039843 | Common:1; Rare:25 | ||||
| chr11:33039952-33040069 | Rare:36 |