| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:114308647-114309005 | Common:2; Rare:66 | ||||
| chr11:114358829-114359045 | Rare:39 | ||||
| chr11:114366940-114367133 | Common:2; Rare:37 | ||||
| chr11:114401805-114401849 | Rare:6 | ||||
| chr11:114448043-114448215 | Rare:34 | ||||
| chr11:115153237-115153366 | Common:1; Rare:25 | ||||
| chr11:115765964-115766164 | Rare:45 | ||||
| chr11:116772380-116772383 | Rare:1 | ||||
| chr11:116773494-116773707 | Common:1; Rare:33 | ||||
| chr11:116808965-116809140 | Common:1; Rare:29 | ||||
| chr11:116809542-116809599 | Rare:10 | ||||
| chr11:116809699-116809733 | Common:2; Rare:7 | ||||
| chr11:116836023-116836348 | Rare:115; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):6 | ||||
| chr11:116871365-116871455 | Rare:19 | ||||
| chr11:116931671-116931866 | Common:1; Rare:44 |