| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:88337580-88338046 | Common:34; Rare:926; Clinvar:45; Clinvar (benign):21 | ||||
| chr11:90222577-90222977 | Common:1; Rare:178 | ||||
| chr11:90222982-90223299 | Common:12; Rare:643 | ||||
| chr11:90223286-90223740 | Common:4; Rare:164 | ||||
| chr11:93196755-93197824 | Common:5; Rare:411 | ||||
| chr11:93197780-93198260 | Common:7; Rare:265 | ||||
| chr11:93330200-93330810 | Common:23; Rare:585 | ||||
| chr11:93543296-93543850 | Common:18; Rare:397 | ||||
| chr11:93661300-93661758 | Common:4; Rare:284 | ||||
| chr11:93661696-93662270 | Common:4; Rare:262 | ||||
| chr11:93735616-93736016 | Common:1; Rare:88 | ||||
| chr11:93737455-93738283 | Rare:229 | ||||
| chr11:93740722-93742293 | Common:57; Rare:1589 | ||||
| chr11:93784022-93784422 | Common:31; Rare:527 | ||||
| chr11:93784740-93785361 | Common:5; Rare:498 |