| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:35525603-35525776 | Rare:43 | ||||
| chr11:36510236-36510372 | Rare:38 | ||||
| chr11:43358814-43358948 | Rare:56 | ||||
| chr11:46617192-46617585 | Common:5; Rare:112 | ||||
| chr11:46846218-46846436 | Common:1; Rare:61 | ||||
| chr11:47214814-47215115 | Common:2; Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248791-47248953 | Rare:67 | ||||
| chr11:47269523-47269684 | Common:1; Rare:54 | ||||
| chr11:47269981-47270166 | Common:1; Rare:61 | ||||
| chr11:47553109-47553347 | Common:1; Rare:80 | ||||
| chr11:47565540-47565635 | Common:2; Rare:15 | ||||
| chr11:47578968-47579114 | Rare:76; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:57324890-57325162 | Common:1; Rare:85 | ||||
| chr11:57335757-57335971 | Common:4; Rare:50 | ||||
| chr11:57530703-57530824 | Common:1; Rare:31 |