| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65639635-65639903 | Rare:46 | ||||
| chr11:65640264-65640511 | Common:2; Rare:42 | ||||
| chr11:65662821-65663362 | Common:4; Rare:129 | ||||
| chr11:65711813-65712125 | Rare:95 | ||||
| chr11:65712156-65712358 | Rare:84 | ||||
| chr11:65712427-65712642 | Common:2; Rare:78 | ||||
| chr11:65720435-65720597 | Common:1; Rare:86 | ||||
| chr11:65720707-65720853 | Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:65780279-65780466 | Common:2; Rare:69 | ||||
| chr11:65780907-65781074 | Rare:71 | ||||
| chr11:65786883-65787065 | Common:2; Rare:22 | ||||
| chr11:65833406-65833689 | Common:4; Rare:65 | ||||
| chr11:65833767-65834015 | Common:1; Rare:54 | ||||
| chr11:65856882-65857430 | Common:4; Rare:168 | ||||
| chr11:65857753-65857948 | Common:1; Rare:74 |