| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65662864-65663039 | Common:1; Rare:45 | ||||
| chr11:65663041-65663390 | Common:3; Rare:82 | ||||
| chr11:65663432-65663594 | Common:2; Rare:33 | ||||
| chr11:65711842-65712073 | Rare:67 | ||||
| chr11:65712153-65712315 | Common:1; Rare:63 | ||||
| chr11:65712358-65712684 | Common:2; Rare:110 | ||||
| chr11:65720463-65720673 | Common:1; Rare:103; Clinvar:1 | ||||
| chr11:65720732-65720853 | Rare:44; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:65779918-65780478 | Common:3; Rare:198 | ||||
| chr11:65780509-65781096 | Common:3; Rare:195 | ||||
| chr11:65856935-65857426 | Common:4; Rare:150 | ||||
| chr11:65857576-65857774 | Common:3; Rare:67 | ||||
| chr11:65857806-65857964 | Rare:61 | ||||
| chr11:65858008-65858749 | Common:3; Rare:209 | ||||
| chr11:65859063-65859116 | Common:1; Rare:11 |