| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:10858013-10858269 | Common:3; Rare:83 | ||||
| chr11:11841859-11842054 | Common:2; Rare:71 | ||||
| chr11:13463159-13463403 | Common:1; Rare:92 | ||||
| chr11:14499779-14499922 | Common:2; Rare:50 | ||||
| chr11:14520314-14520575 | Rare:83 | ||||
| chr11:14891645-14891811 | Rare:44 | ||||
| chr11:14892134-14892397 | Rare:97 | ||||
| chr11:16738413-16738707 | Common:3; Rare:70 | ||||
| chr11:17077618-17077893 | Common:2; Rare:118 | ||||
| chr11:17207920-17208128 | Common:1; Rare:81 | ||||
| chr11:17276537-17276816 | Common:4; Rare:80; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:18012925-18013269 | Common:6; Rare:115 | ||||
| chr11:18322108-18322317 | Common:3; Rare:80; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322447-18322631 | Common:2; Rare:72 | ||||
| chr11:18394422-18394636 | Common:1; Rare:84; Clinvar (benign):1 |