| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33774501-33774670 | Common:2; Rare:62 | ||||
| chr11:34105442-34105661 | Common:4; Rare:70 | ||||
| chr11:34438784-34438983 | Common:1; Rare:66 | ||||
| chr11:34916302-34916676 | Common:10; Rare:152; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35139018-35139275 | Common:1; Rare:58 | ||||
| chr11:36510240-36510361 | Rare:34 | ||||
| chr11:43358885-43358979 | Rare:51 | ||||
| chr11:46700568-46700796 | Common:1; Rare:61 | ||||
| chr11:46846224-46846432 | Common:1; Rare:58 | ||||
| chr11:47269966-47270150 | Common:1; Rare:59 | ||||
| chr11:47565522-47565620 | Common:2; Rare:18 | ||||
| chr11:47578940-47579097 | Rare:82; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:57530682-57530807 | Rare:34 | ||||
| chr11:57712183-57712621 | Common:9; Rare:144 | ||||
| chr11:57741283-57741596 | Common:1; Rare:117 |