| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:129835175-129835481 | Common:3; Rare:124 | ||||
| chr9:130053876-130053983 | Common:1; Rare:50 | ||||
| chr9:130693597-130693789 | Rare:62 | ||||
| chr9:131125446-131125707 | Common:1; Rare:122 | ||||
| chr9:131502885-131503040 | Rare:55; Clinvar:3 | ||||
| chr9:131531170-131531371 | Common:9; Rare:93 | ||||
| chr9:132354932-132355246 | Common:4; Rare:104 | ||||
| chr9:132669930-132670063 | Common:1; Rare:60 | ||||
| chr9:132878823-132878954 | Rare:23 | ||||
| chr9:133348043-133348276 | Common:2; Rare:98 | ||||
| chr9:133348614-133349042 | Common:5; Rare:180 | ||||
| chr9:133356458-133356599 | Common:1; Rare:64; Clinvar (benign):2 | ||||
| chr9:133375965-133376332 | Common:3; Rare:134 | ||||
| chr9:135961182-135961538 | Common:6; Rare:127 | ||||
| chr9:136410609-136410678 | Rare:34 |