| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:22625808-22626009 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:22829298-22829422 | Common:1; Rare:29 | ||||
| chr11:22829693-22829925 | Common:3; Rare:89 | ||||
| chr11:22860403-22860540 | Common:1; Rare:40 | ||||
| chr11:26332015-26332137 | Common:2; Rare:38 | ||||
| chr11:27362836-27363323 | Common:2; Rare:203 | ||||
| chr11:27472736-27472848 | Common:1; Rare:26 | ||||
| chr11:27506730-27506886 | Common:1; Rare:71 | ||||
| chr11:28108120-28108451 | Common:2; Rare:101 | ||||
| chr11:30322918-30323169 | Common:2; Rare:72 | ||||
| chr11:31369698-31369887 | Rare:55 | ||||
| chr11:31509526-31509954 | Common:2; Rare:157 | ||||
| chr11:31816110-31816151 | Rare:10 | ||||
| chr11:32430670-32430968 | Common:4; Rare:64 | ||||
| chr11:32434918-32435239 | Common:2; Rare:113; Clinvar:25; Clinvar (benign):9; Clinvar (pathogenic):1 |