| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46345211-46345450 | Common:1; Rare:72 | ||||
| chr11:46617175-46617607 | Common:5; Rare:124 | ||||
| chr11:46700551-46701070 | Common:4; Rare:132 | ||||
| chr11:46846218-46846414 | Common:1; Rare:54 | ||||
| chr11:47176849-47177149 | Common:1; Rare:122 | ||||
| chr11:47186408-47186528 | Rare:33 | ||||
| chr11:47269566-47269690 | Common:1; Rare:41 | ||||
| chr11:47269981-47270188 | Common:1; Rare:69 | ||||
| chr11:47553090-47553356 | Common:2; Rare:91 | ||||
| chr11:47565478-47565643 | Common:3; Rare:32 | ||||
| chr11:47578958-47579094 | Rare:69; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:57324860-57325148 | Common:2; Rare:91 | ||||
| chr11:57530692-57531074 | Common:1; Rare:92 | ||||
| chr11:57711974-57712629 | Common:10; Rare:217 | ||||
| chr11:58578101-58578104 | Rare:1 |