| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:94726547-94726734 | Rare:53 | ||||
| chr9:95507389-95507659 | Rare:82 | ||||
| chr9:95509131-95509211 | Rare:22 | ||||
| chr9:95875453-95875731 | Common:1; Rare:98 | ||||
| chr9:95875968-95876084 | Common:5; Rare:59; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:96566879-96567167 | Rare:72 | ||||
| chr9:96655289-96655408 | Rare:32 | ||||
| chr9:96778054-96778159 | Rare:33 | ||||
| chr9:97039130-97039282 | Rare:55 | ||||
| chr9:97633267-97633872 | Common:6; Rare:187 | ||||
| chr9:97666681-97666827 | Common:1; Rare:30 | ||||
| chr9:97922471-97922607 | Common:3; Rare:64 | ||||
| chr9:97983174-97983590 | Common:2; Rare:161 | ||||
| chr9:97984494-97984589 | Common:1; Rare:49 | ||||
| chr9:98056393-98056938 | Common:7; Rare:182 |