| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14520298-14520594 | Rare:99 | ||||
| chr11:16738466-16738709 | Common:3; Rare:53 | ||||
| chr11:17207920-17208093 | Common:1; Rare:67 | ||||
| chr11:17276470-17276816 | Common:4; Rare:102; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:18322158-18322312 | Common:1; Rare:47 | ||||
| chr11:18322437-18322607 | Common:2; Rare:66 | ||||
| chr11:18394409-18394574 | Common:1; Rare:60; Clinvar (benign):1 | ||||
| chr11:18526841-18527063 | Common:2; Rare:105 | ||||
| chr11:18588679-18588809 | Rare:41 | ||||
| chr11:18634332-18634574 | Common:2; Rare:77 | ||||
| chr11:27472762-27472781 | Rare:4 | ||||
| chr11:27506751-27506859 | Common:1; Rare:46 | ||||
| chr11:28108120-28108363 | Rare:71 | ||||
| chr11:31369737-31369882 | Rare:45 | ||||
| chr11:31509575-31509790 | Common:1; Rare:67 |