| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66002458-66002826 | Common:2; Rare:183; Clinvar:2 | ||||
| chr11:66051754-66052587 | Common:19; Rare:460 | ||||
| chr11:66070006-66070442 | Common:4; Rare:243 | ||||
| chr11:66070760-66071300 | Common:5; Rare:185; Clinvar (benign):2 | ||||
| chr11:66257568-66257848 | Rare:157 | ||||
| chr11:66258355-66258483 | Rare:25 | ||||
| chr11:66258388-66258694 | Rare:82 | ||||
| chr11:66268404-66268689 | Common:6; Rare:157 | ||||
| chr11:66288966-66289457 | Common:3; Rare:241 | ||||
| chr11:66341150-66341830 | Common:4; Rare:204 | ||||
| chr11:66345008-66345254 | Common:2; Rare:112 | ||||
| chr11:66347611-66347942 | Common:9; Rare:124 | ||||
| chr11:66347980-66348290 | Common:2; Rare:233 | ||||
| chr11:66371227-66371536 | Rare:182 | ||||
| chr11:66371524-66372340 | Common:9; Rare:394 |