| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65110585-65110725 | Rare:40 | ||||
| chr11:65134507-65134612 | Common:1; Rare:21 | ||||
| chr11:65181874-65181972 | Rare:18 | ||||
| chr11:65314685-65314904 | Rare:69 | ||||
| chr11:65333637-65333911 | Common:1; Rare:122 | ||||
| chr11:65386495-65386657 | Rare:50 | ||||
| chr11:65570411-65570504 | Rare:43 | ||||
| chr11:65638062-65638133 | Common:2; Rare:27 | ||||
| chr11:65662884-65663104 | Common:1; Rare:56 | ||||
| chr11:65711869-65712018 | Rare:47 | ||||
| chr11:65712224-65712258 | Rare:11 | ||||
| chr11:65860366-65860436 | Common:1; Rare:22 | ||||
| chr11:65888372-65888637 | Common:1; Rare:94 | ||||
| chr11:65961539-65961764 | Rare:77 | ||||
| chr11:66002127-66002552 | Common:3; Rare:120; Clinvar:3; Clinvar (benign):3 |