| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:28108115-28108396 | Common:1; Rare:84 | ||||
| chr11:31369737-31369870 | Rare:43 | ||||
| chr11:31509606-31509787 | Common:1; Rare:55 | ||||
| chr11:32583663-32583859 | Rare:73 | ||||
| chr11:33736410-33736605 | Common:1; Rare:64 | ||||
| chr11:34916322-34916650 | Common:9; Rare:134; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr11:35139002-35139182 | Common:1; Rare:44 | ||||
| chr11:36510261-36510372 | Rare:33 | ||||
| chr11:47565516-47565615 | Common:1; Rare:18 | ||||
| chr11:47578959-47579085 | Rare:65; Clinvar:2 | ||||
| chr11:57712204-57712272 | Common:6; Rare:41 | ||||
| chr11:57712282-57712618 | Common:3; Rare:91 | ||||
| chr11:57741405-57741588 | Rare:71 | ||||
| chr11:59142692-59142945 | Common:1; Rare:45 | ||||
| chr11:60906507-60906795 | Rare:73 |