| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:74949086-74949288 | Common:6; Rare:50 | ||||
| chr11:75562073-75562297 | Common:1; Rare:57; Clinvar:4; Clinvar (benign):2 | ||||
| chr11:76381112-76381348 | Common:3; Rare:74 | ||||
| chr11:76444660-76445050 | Common:1; Rare:89 | ||||
| chr11:76783065-76783367 | Common:8; Rare:99 | ||||
| chr11:76860669-76860959 | Common:4; Rare:92 | ||||
| chr11:77637739-77637866 | Common:1; Rare:49 | ||||
| chr11:77820840-77821183 | Common:2; Rare:100 | ||||
| chr11:78139590-78139808 | Common:3; Rare:87; Clinvar:2 | ||||
| chr11:83071836-83072103 | Common:3; Rare:76 | ||||
| chr11:83193662-83193750 | Common:1; Rare:33 | ||||
| chr11:83285948-83286092 | Common:2; Rare:61 | ||||
| chr11:85628339-85628605 | Common:6; Rare:80 | ||||
| chr11:85647875-85647991 | Rare:26; Clinvar:2 | ||||
| chr11:88337668-88337847 | Common:4; Rare:92; Clinvar:6; Clinvar (benign):3 |