| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:116733106-116733506 | Common:7; Rare:171 | ||||
| chr11:116734129-116734279 | Rare:29 | ||||
| chr11:116782681-116783144 | Common:2; Rare:170 | ||||
| chr11:116835280-116835428 | Common:1; Rare:33 | ||||
| chr11:116835976-116836218 | Rare:93; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):6 | ||||
| chr11:116852695-116853095 | Common:3; Rare:99 | ||||
| chr11:116853593-116853849 | Rare:44 | ||||
| chr11:116930209-116930362 | Common:2; Rare:28 | ||||
| chr11:116981453-116981853 | Common:1; Rare:133 | ||||
| chr11:117019862-117020684 | Common:28; Rare:218 | ||||
| chr11:117063249-117063433 | Common:1; Rare:30 | ||||
| chr11:117093143-117093543 | Common:10; Rare:93 | ||||
| chr11:117095287-117095499 | Common:2; Rare:35 | ||||
| chr11:117096597-117096768 | Rare:54 | ||||
| chr11:117145060-117145485 | Common:4; Rare:206 |