| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65181255-65181491 | Common:1; Rare:56 | ||||
| chr11:65181783-65181972 | Common:1; Rare:39 | ||||
| chr11:65261390-65261521 | Rare:21 | ||||
| chr11:65261648-65262223 | Common:6; Rare:169 | ||||
| chr11:65262281-65262464 | Rare:63 | ||||
| chr11:65314680-65315137 | Rare:123 | ||||
| chr11:65333607-65333957 | Common:1; Rare:144 | ||||
| chr11:65334104-65334256 | Rare:35 | ||||
| chr11:65354461-65354838 | Common:1; Rare:113 | ||||
| chr11:65382274-65382736 | Common:3; Rare:94 | ||||
| chr11:65382752-65382797 | Rare:4 | ||||
| chr11:65386525-65386701 | Rare:58 | ||||
| chr11:65503216-65503699 | Common:2; Rare:216 | ||||
| chr11:65524788-65525156 | Rare:72 | ||||
| chr11:65539957-65540347 | Rare:151; Clinvar (benign):1; Clinvar (pathogenic):1 |