| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34179250-34179466 | Rare:40 | ||||
| chr9:34329228-34329638 | Common:1; Rare:122 | ||||
| chr9:34457221-34457452 | Rare:41 | ||||
| chr9:34458527-34458892 | Common:2; Rare:92; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:34590119-34590183 | Common:1; Rare:13 | ||||
| chr9:34612064-34612223 | Common:9; Rare:58 | ||||
| chr9:34620417-34620651 | Common:1; Rare:67 | ||||
| chr9:34637759-34638009 | Common:2; Rare:70 | ||||
| chr9:34638088-34638166 | Rare:16 | ||||
| chr9:34646484-34646804 | Common:1; Rare:98; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr9:34651909-34652217 | Rare:89 | ||||
| chr9:34665976-34666196 | Common:3; Rare:59 | ||||
| chr9:34989348-34989831 | Common:2; Rare:124 | ||||
| chr9:34990020-34990462 | Common:1; Rare:129 | ||||
| chr9:34991219-34991370 | Rare:27 |