| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:130043028-130043320 | Common:2; Rare:92 | ||||
| chr9:130053846-130053940 | Common:1; Rare:31 | ||||
| chr9:131096274-131096590 | Common:3; Rare:85 | ||||
| chr9:131125407-131125637 | Common:2; Rare:105 | ||||
| chr9:131502879-131503040 | Rare:55; Clinvar:3 | ||||
| chr9:132669930-132670065 | Common:1; Rare:61 | ||||
| chr9:132670289-132670491 | Rare:57 | ||||
| chr9:133348043-133348266 | Common:2; Rare:90 | ||||
| chr9:133348752-133349042 | Common:2; Rare:115 | ||||
| chr9:133356443-133356616 | Common:1; Rare:81; Clinvar (benign):2 | ||||
| chr9:133375999-133376366 | Common:1; Rare:133 | ||||
| chr9:133417907-133418086 | Common:2; Rare:49 | ||||
| chr9:134371850-134371962 | Rare:29 | ||||
| chr9:134641547-134641809 | Common:2; Rare:82; Clinvar (benign):1 | ||||
| chr9:136410382-136410670 | Common:6; Rare:122 |