| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:30920023-30920173 | Common:2; Rare:21 | ||||
| chr11:31120676-31121076 | Rare:87 | ||||
| chr11:31141701-31142201 | Common:4; Rare:159 | ||||
| chr11:31238541-31238685 | Rare:22 | ||||
| chr11:31240274-31240674 | Common:1; Rare:101 | ||||
| chr11:31674644-31675044 | Common:4; Rare:107 | ||||
| chr11:31788096-31788496 | Rare:123; Clinvar:2; Clinvar (benign):5 | ||||
| chr11:31795885-31796653 | Common:1; Rare:196 | ||||
| chr11:31808689-31809089 | Common:3; Rare:92 | ||||
| chr11:31809344-31809744 | Common:1; Rare:101 | ||||
| chr11:31814965-31815103 | Common:4; Rare:31 | ||||
| chr11:31875830-31876043 | Common:2; Rare:34 | ||||
| chr11:31876170-31876640 | Common:2; Rare:94 | ||||
| chr11:31883003-31883403 | Common:2; Rare:106 | ||||
| chr11:32527216-32527717 | Common:1; Rare:165 |