| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:96282150-96282186 | Rare:7 | ||||
| chr9:96293853-96293974 | Common:1; Rare:21 | ||||
| chr9:96417399-96417745 | Common:3; Rare:90 | ||||
| chr9:96451053-96451179 | Rare:27 | ||||
| chr9:96686888-96687089 | Common:3; Rare:56 | ||||
| chr9:96700159-96700302 | Common:1; Rare:37 | ||||
| chr9:97221498-97221703 | Common:6; Rare:51 | ||||
| chr9:97238359-97238525 | Common:1; Rare:41 | ||||
| chr9:97238670-97238910 | Common:2; Rare:57 | ||||
| chr9:97341773-97341967 | Common:3; Rare:37 | ||||
| chr9:97396662-97396752 | Common:1; Rare:11 | ||||
| chr9:97468263-97468411 | Common:1; Rare:19 | ||||
| chr9:97516447-97516510 | Common:1; Rare:8 | ||||
| chr9:97662669-97663046 | Rare:80 | ||||
| chr9:97687184-97687456 | Common:1; Rare:62; Clinvar:1; Clinvar (pathogenic):2 |