| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65134470-65134596 | Common:1; Rare:34 | ||||
| chr11:65181283-65181394 | Common:1; Rare:25 | ||||
| chr11:65261761-65262029 | Common:2; Rare:76 | ||||
| chr11:65314704-65314913 | Rare:71 | ||||
| chr11:65333617-65333898 | Common:1; Rare:119 | ||||
| chr11:65386495-65386687 | Rare:63 | ||||
| chr11:65524807-65525147 | Rare:64 | ||||
| chr11:65546515-65546832 | Common:3; Rare:106; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:65570402-65570504 | Rare:47 | ||||
| chr11:65575843-65576029 | Common:3; Rare:54 | ||||
| chr11:65614186-65614335 | Rare:35 | ||||
| chr11:65615496-65615830 | Common:1; Rare:119 | ||||
| chr11:65638011-65638180 | Common:3; Rare:75 | ||||
| chr11:65662795-65663093 | Common:1; Rare:72 | ||||
| chr11:65711967-65712262 | Common:1; Rare:100 |