| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47214832-47215011 | Common:1; Rare:43 | ||||
| chr11:47248774-47248944 | Rare:69 | ||||
| chr11:47269966-47270202 | Common:1; Rare:83 | ||||
| chr11:47426423-47426632 | Rare:52 | ||||
| chr11:47565500-47565635 | Common:3; Rare:24 | ||||
| chr11:47578965-47579106 | Rare:70; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642473-47642819 | Rare:126 | ||||
| chr11:57324883-57325164 | Common:1; Rare:94 | ||||
| chr11:57514858-57514970 | Rare:20 | ||||
| chr11:57606187-57606547 | Rare:91 | ||||
| chr11:57657522-57657790 | Common:4; Rare:67 | ||||
| chr11:57712178-57712704 | Common:9; Rare:184 | ||||
| chr11:57741255-57741590 | Common:1; Rare:129 | ||||
| chr11:57753154-57753299 | Rare:29 | ||||
| chr11:58578100-58578537 | Common:4; Rare:139 |