| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65386460-65386737 | Common:1; Rare:146 | ||||
| chr11:65524760-65525163 | Rare:77 | ||||
| chr11:65525240-65525710 | Rare:195 | ||||
| chr11:65540616-65540796 | Common:6; Rare:117 | ||||
| chr11:65546550-65546970 | Common:6; Rare:232; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr11:65558150-65558710 | Common:8; Rare:150 | ||||
| chr11:65569890-65570170 | Common:2; Rare:149 | ||||
| chr11:65570271-65570753 | Common:4; Rare:330 | ||||
| chr11:65575837-65576132 | Common:3; Rare:84 | ||||
| chr11:65614167-65614468 | Rare:127 | ||||
| chr11:65615130-65615629 | Common:2; Rare:263 | ||||
| chr11:65615561-65615859 | Common:3; Rare:149 | ||||
| chr11:65616023-65616370 | Common:2; Rare:223 | ||||
| chr11:65637996-65638257 | Common:7; Rare:157 | ||||
| chr11:65662834-65663031 | Common:2; Rare:83 |