| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:131373404-131373683 | Common:1; Rare:62 | ||||
| chr9:131454401-131454622 | Common:1; Rare:43 | ||||
| chr9:131987087-131987172 | Rare:14 | ||||
| chr9:132296719-132296920 | Common:1; Rare:58; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr9:132313851-132313929 | Rare:17 | ||||
| chr9:133351420-133351672 | Common:1; Rare:77 | ||||
| chr9:133360036-133360307 | Common:3; Rare:101 | ||||
| chr9:133419191-133419293 | Rare:22 | ||||
| chr9:133430729-133430746 | Rare:3 | ||||
| chr9:133785606-133785837 | Common:1; Rare:37 | ||||
| chr9:133791830-133791956 | Rare:31 | ||||
| chr9:135476691-135476993 | Common:3; Rare:68 | ||||
| chr9:136051845-136051889 | Rare:14 | ||||
| chr9:136484538-136485078 | Rare:196 | ||||
| chr9:136724718-136724773 | Common:1; Rare:17 |