| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34049175-34049263 | Common:1; Rare:22 | ||||
| chr9:34178780-34179096 | Common:1; Rare:81 | ||||
| chr9:34179258-34179529 | Rare:54 | ||||
| chr9:34329186-34329604 | Rare:133 | ||||
| chr9:34612071-34612223 | Common:8; Rare:54 | ||||
| chr9:34637681-34637924 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:34652015-34652207 | Rare:55 | ||||
| chr9:34665373-34665660 | Rare:94 | ||||
| chr9:34666026-34666067 | Rare:8 | ||||
| chr9:35072371-35072675 | Rare:82; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35079672-35079775 | Rare:19 | ||||
| chr9:35079917-35080153 | Common:4; Rare:58; Clinvar:3; Clinvar (benign):3 | ||||
| chr9:35103090-35103198 | Common:1; Rare:37 | ||||
| chr9:35161828-35162124 | Common:4; Rare:85 | ||||
| chr9:35162153-35162215 | Rare:15 |