| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18322459-18322703 | Common:2; Rare:88 | ||||
| chr11:18394408-18394631 | Common:1; Rare:87; Clinvar (benign):1 | ||||
| chr11:18526841-18526977 | Rare:66 | ||||
| chr11:18588661-18588929 | Common:3; Rare:90 | ||||
| chr11:18634317-18634588 | Common:2; Rare:88 | ||||
| chr11:18698653-18698773 | Common:2; Rare:35 | ||||
| chr11:20363659-20363788 | Common:3; Rare:28 | ||||
| chr11:20387417-20387671 | Common:7; Rare:82 | ||||
| chr11:22625806-22626002 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:26994050-26994176 | Common:1; Rare:18 | ||||
| chr11:26994378-26994617 | Common:1; Rare:62 | ||||
| chr11:27363121-27363296 | Rare:77 | ||||
| chr11:27506721-27506868 | Common:1; Rare:69 | ||||
| chr11:28108130-28108414 | Common:1; Rare:83 | ||||
| chr11:30322966-30323183 | Common:2; Rare:61 |