| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:129110667-129111029 | Common:5; Rare:114 | ||||
| chr9:129752982-129753173 | Common:1; Rare:55 | ||||
| chr9:129835145-129835481 | Common:3; Rare:134 | ||||
| chr9:130043086-130043305 | Common:2; Rare:68 | ||||
| chr9:130053854-130053978 | Common:1; Rare:52 | ||||
| chr9:130451929-130452240 | Common:2; Rare:86; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr9:130579456-130579683 | Common:6; Rare:98 | ||||
| chr9:131125446-131125651 | Common:1; Rare:99 | ||||
| chr9:131502860-131503033 | Rare:63; Clinvar:3 | ||||
| chr9:131531182-131531363 | Common:9; Rare:82 | ||||
| chr9:132354922-132355281 | Common:5; Rare:117 | ||||
| chr9:132669930-132670078 | Common:1; Rare:66 | ||||
| chr9:132878279-132878408 | Common:1; Rare:49 | ||||
| chr9:132878838-132878945 | Rare:16 | ||||
| chr9:133348024-133348276 | Common:3; Rare:103 |