| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:103092028-103092242 | Common:1; Rare:62 | ||||
| chr11:106077326-106077711 | Common:2; Rare:115 | ||||
| chr11:107859186-107859300 | Rare:26 | ||||
| chr11:108008543-108009242 | Common:1; Rare:154 | ||||
| chr11:108009260-108009363 | Rare:49 | ||||
| chr11:108134043-108134315 | Common:2; Rare:61; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr11:108222551-108223127 | Common:1; Rare:189; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:111299032-111299157 | Common:1; Rare:26 | ||||
| chr11:111299629-111299776 | Common:2; Rare:37 | ||||
| chr11:111602168-111602579 | Common:1; Rare:132 | ||||
| chr11:111766327-111766433 | Common:1; Rare:67 | ||||
| chr11:111871240-111871376 | Common:1; Rare:47; Clinvar:1 | ||||
| chr11:111878862-111879016 | Common:2; Rare:64 | ||||
| chr11:111879147-111879548 | Common:1; Rare:125 | ||||
| chr11:111912708-111912765 | Rare:6 |