| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33161435-33161632 | Common:6; Rare:53 | ||||
| chr11:33257195-33257427 | Common:3; Rare:78 | ||||
| chr11:34916328-34916658 | Common:10; Rare:132; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35138962-35139184 | Common:1; Rare:52 | ||||
| chr11:35525581-35525821 | Rare:58 | ||||
| chr11:36510236-36510372 | Rare:38 | ||||
| chr11:43358845-43358979 | Rare:62 | ||||
| chr11:46120952-46121291 | Common:2; Rare:54 | ||||
| chr11:46617222-46617585 | Common:5; Rare:99 | ||||
| chr11:46700559-46700872 | Common:1; Rare:85 | ||||
| chr11:46846220-46846414 | Common:1; Rare:54 | ||||
| chr11:47185346-47185694 | Common:2; Rare:68 | ||||
| chr11:47186347-47186544 | Rare:56 | ||||
| chr11:47269981-47270166 | Common:1; Rare:61 | ||||
| chr11:47565490-47565625 | Common:3; Rare:27 |