| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:30322971-30323154 | Common:1; Rare:53 | ||||
| chr11:31509566-31509790 | Common:1; Rare:69 | ||||
| chr11:33161449-33161682 | Common:6; Rare:65 | ||||
| chr11:34052126-34052368 | Common:2; Rare:107 | ||||
| chr11:34916318-34916653 | Common:10; Rare:135; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:36510249-36510362 | Rare:30 | ||||
| chr11:43880705-43880863 | Common:1; Rare:32 | ||||
| chr11:46700568-46700860 | Common:1; Rare:77 | ||||
| chr11:47565490-47565620 | Common:3; Rare:26 | ||||
| chr11:47578966-47579087 | Rare:62; Clinvar:2 | ||||
| chr11:57712192-57712621 | Common:9; Rare:142 | ||||
| chr11:60906511-60906737 | Rare:59 | ||||
| chr11:61333032-61333266 | Rare:82 | ||||
| chr11:61361842-61362105 | Common:2; Rare:65; Clinvar:3 | ||||
| chr11:61362276-61362397 | Common:1; Rare:34; Clinvar:5 |