| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65422673-65422804 | Common:1; Rare:40 | ||||
| chr11:65455142-65455318 | Rare:72 | ||||
| chr11:65497395-65497837 | Common:1; Rare:192 | ||||
| chr11:65500556-65501094 | Common:2; Rare:259 | ||||
| chr11:65526000-65526278 | Rare:94; Clinvar (pathogenic):1 | ||||
| chr11:66557819-66558077 | Common:1; Rare:94 | ||||
| chr11:67619820-67620166 | Common:4; Rare:79 | ||||
| chr11:67620206-67620293 | Common:1; Rare:23 | ||||
| chr11:67620840-67621038 | Common:1; Rare:34 | ||||
| chr11:67744391-67744613 | Common:1; Rare:54 | ||||
| chr11:67790226-67790305 | Rare:27 | ||||
| chr11:67805302-67805617 | Common:3; Rare:114 | ||||
| chr11:68036605-68036674 | Common:2; Rare:23; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:68879409-68879562 | Common:1; Rare:24 | ||||
| chr11:72018396-72018649 | Common:1; Rare:72 |