| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:35525713-35525943 | Common:2; Rare:43 | ||||
| chr11:35662603-35662907 | Common:3; Rare:92 | ||||
| chr11:35943958-35944131 | Common:2; Rare:62 | ||||
| chr11:36510229-36510372 | Rare:43 | ||||
| chr11:43358813-43359047 | Rare:103 | ||||
| chr11:45847232-45847487 | Common:2; Rare:104 | ||||
| chr11:46594006-46594133 | Common:1; Rare:27 | ||||
| chr11:46617165-46617585 | Common:5; Rare:118 | ||||
| chr11:46846218-46846394 | Rare:46 | ||||
| chr11:47269556-47269714 | Common:1; Rare:55 | ||||
| chr11:47426416-47426648 | Rare:55 | ||||
| chr11:47565478-47565620 | Common:3; Rare:28 | ||||
| chr11:47578920-47579113 | Rare:101; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47848314-47848406 | Rare:49 | ||||
| chr11:57324890-57325173 | Common:1; Rare:87 |