| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65614980-65615409 | Common:1; Rare:98 | ||||
| chr11:65615566-65615675 | Rare:38 | ||||
| chr11:65615704-65615871 | Common:1; Rare:54 | ||||
| chr11:65616019-65616151 | Rare:33 | ||||
| chr11:65637978-65638241 | Common:4; Rare:98 | ||||
| chr11:65647237-65647402 | Rare:54 | ||||
| chr11:65662700-65662746 | Rare:16 | ||||
| chr11:65662868-65663526 | Common:5; Rare:159 | ||||
| chr11:65711162-65711522 | Common:2; Rare:71 | ||||
| chr11:65711822-65712315 | Common:1; Rare:171 | ||||
| chr11:65712463-65712684 | Common:2; Rare:81 | ||||
| chr11:65720277-65720623 | Common:3; Rare:158; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:65720625-65720853 | Rare:92; Clinvar:4; Clinvar (benign):2 | ||||
| chr11:65780311-65780384 | Rare:30 | ||||
| chr11:65780447-65780705 | Common:1; Rare:75 |