| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64359054-64359177 | Rare:30 | ||||
| chr11:64759776-64760126 | Rare:104; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr11:64778419-64778698 | Common:2; Rare:127 | ||||
| chr11:64778761-64778894 | Common:1; Rare:52 | ||||
| chr11:64803152-64803344 | Rare:78 | ||||
| chr11:64878480-64878833 | Common:4; Rare:135 | ||||
| chr11:64917275-64917573 | Common:3; Rare:61 | ||||
| chr11:65014011-65014254 | Rare:64 | ||||
| chr11:65084028-65084302 | Common:1; Rare:87 | ||||
| chr11:65117625-65117778 | Common:1; Rare:74 | ||||
| chr11:65134489-65134636 | Common:1; Rare:36 | ||||
| chr11:65181281-65181398 | Common:1; Rare:26 | ||||
| chr11:65181817-65182012 | Rare:41 | ||||
| chr11:65261746-65262062 | Common:3; Rare:90 | ||||
| chr11:65333776-65333890 | Common:1; Rare:61 |