| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:43880680-43880877 | Common:2; Rare:45 | ||||
| chr11:44066100-44066272 | Common:3; Rare:48 | ||||
| chr11:45286249-45286432 | Rare:52 | ||||
| chr11:46120952-46121259 | Common:2; Rare:46 | ||||
| chr11:46593994-46594133 | Common:2; Rare:29 | ||||
| chr11:46617245-46617585 | Common:5; Rare:94 | ||||
| chr11:46700555-46700818 | Common:1; Rare:68 | ||||
| chr11:46846211-46846422 | Common:1; Rare:61 | ||||
| chr11:47186408-47186529 | Rare:33 | ||||
| chr11:47214837-47215123 | Common:2; Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47269523-47269684 | Common:1; Rare:54 | ||||
| chr11:47269986-47270150 | Common:1; Rare:55 | ||||
| chr11:47553109-47553341 | Common:1; Rare:78 | ||||
| chr11:47565540-47565637 | Common:2; Rare:15 | ||||
| chr11:47578959-47579087 | Rare:66; Clinvar:2 |