| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:75088892-75088962 | Rare:11 | ||||
| chr9:75890570-75890686 | Rare:42 | ||||
| chr9:76459076-76459234 | Common:1; Rare:57 | ||||
| chr9:78236001-78236107 | Rare:34 | ||||
| chr9:78296855-78297203 | Common:2; Rare:98; Clinvar (benign):1 | ||||
| chr9:79572443-79572729 | Common:1; Rare:103 | ||||
| chr9:81689403-81689853 | Common:11; Rare:172 | ||||
| chr9:83622919-83623155 | Common:3; Rare:51 | ||||
| chr9:83707543-83707550 | Rare:1 | ||||
| chr9:83707658-83708349 | Common:6; Rare:236 | ||||
| chr9:83921405-83921591 | Common:2; Rare:76 | ||||
| chr9:83979574-83979691 | Rare:43 | ||||
| chr9:83980135-83980400 | Common:2; Rare:101 | ||||
| chr9:83980502-83980844 | Common:5; Rare:141 | ||||
| chr9:84669549-84669791 | Common:2; Rare:52 |