| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:20387456-20387733 | Common:7; Rare:88 | ||||
| chr11:22625122-22625261 | Common:2; Rare:62; Clinvar:4; Clinvar (benign):5 | ||||
| chr11:22625807-22626002 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:22829713-22829983 | Common:3; Rare:107 | ||||
| chr11:27506721-27506863 | Common:1; Rare:65 | ||||
| chr11:28108113-28108396 | Common:1; Rare:85 | ||||
| chr11:31369737-31369911 | Rare:53 | ||||
| chr11:31509576-31509806 | Common:1; Rare:76 | ||||
| chr11:33039535-33039782 | Common:1; Rare:60 | ||||
| chr11:33161419-33161565 | Common:4; Rare:41 | ||||
| chr11:34052069-34052368 | Common:3; Rare:130 | ||||
| chr11:34105429-34105645 | Common:4; Rare:63 | ||||
| chr11:34438766-34439011 | Common:2; Rare:82; Clinvar (benign):1 | ||||
| chr11:34916326-34916458 | Common:4; Rare:50; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:35139112-35139202 | Rare:12 |