| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128456696-128456984 | Common:2; Rare:80 | ||||
| chr9:128504581-128504793 | Rare:98; Clinvar:5 | ||||
| chr9:128552383-128552611 | Rare:84; Clinvar:1 | ||||
| chr9:128656652-128656840 | Common:2; Rare:80; Clinvar (pathogenic):1 | ||||
| chr9:128683259-128683434 | Common:5; Rare:25 | ||||
| chr9:128683496-128683890 | Rare:87 | ||||
| chr9:128724081-128724475 | Common:3; Rare:129 | ||||
| chr9:128771831-128772024 | Rare:51 | ||||
| chr9:128881907-128882213 | Common:2; Rare:104 | ||||
| chr9:128921983-128922346 | Common:2; Rare:86 | ||||
| chr9:128947573-128947747 | Common:2; Rare:81; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:129110653-129110953 | Common:3; Rare:68 | ||||
| chr9:129111224-129111593 | Common:2; Rare:105 | ||||
| chr9:129139884-129140150 | Rare:61 | ||||
| chr9:129626113-129626193 | Rare:31 |