| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:10455134-10455385 | Common:5; Rare:43; Clinvar:1; Clinvar (benign):6 | ||||
| chr11:10858030-10858223 | Common:2; Rare:50 | ||||
| chr11:11841949-11842016 | Common:1; Rare:24 | ||||
| chr11:16738466-16738689 | Common:2; Rare:45 | ||||
| chr11:17077628-17077965 | Common:2; Rare:139 | ||||
| chr11:17207922-17208064 | Common:1; Rare:54 | ||||
| chr11:17276475-17276804 | Common:4; Rare:95; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:18322128-18322279 | Common:3; Rare:49; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322521-18322610 | Common:1; Rare:42 | ||||
| chr11:18394459-18394612 | Common:1; Rare:62; Clinvar (benign):1 | ||||
| chr11:18526841-18527025 | Common:1; Rare:94 | ||||
| chr11:18634353-18634588 | Common:1; Rare:75 | ||||
| chr11:27506753-27506838 | Common:1; Rare:38 | ||||
| chr11:31509592-31509784 | Common:1; Rare:61 | ||||
| chr11:33161449-33161764 | Common:6; Rare:86 |