| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34329204-34329598 | Rare:124 | ||||
| chr9:34376858-34377089 | Rare:55 | ||||
| chr9:34458527-34458826 | Common:1; Rare:72 | ||||
| chr9:34612073-34612223 | Common:8; Rare:54 | ||||
| chr9:34637725-34637953 | Rare:67 | ||||
| chr9:34638010-34638125 | Common:1; Rare:19 | ||||
| chr9:34646506-34646804 | Common:1; Rare:94; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr9:34652015-34652207 | Rare:55 | ||||
| chr9:34665351-34665665 | Rare:98 | ||||
| chr9:34665996-34666139 | Common:1; Rare:33 | ||||
| chr9:35071975-35072320 | Common:1; Rare:118 | ||||
| chr9:35072442-35072675 | Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:35102811-35103220 | Common:1; Rare:124 | ||||
| chr9:35161819-35162167 | Common:4; Rare:99 | ||||
| chr9:35162286-35162304 | Rare:5 |