| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:16870655-16871076 | Common:4; Rare:164 | ||||
| chr9:18473929-18474231 | Rare:83 | ||||
| chr9:19049331-19049463 | Rare:61 | ||||
| chr9:19049687-19050203 | Common:2; Rare:102 | ||||
| chr9:19102859-19103056 | Common:2; Rare:82 | ||||
| chr9:19127420-19127797 | Common:7; Rare:112 | ||||
| chr9:19230652-19230836 | Common:3; Rare:90 | ||||
| chr9:19376288-19376642 | Common:2; Rare:129 | ||||
| chr9:19380171-19380367 | Common:5; Rare:97 | ||||
| chr9:19408672-19409014 | Common:7; Rare:118 | ||||
| chr9:20684108-20684313 | Common:3; Rare:78 | ||||
| chr9:21803271-21803308 | Rare:8 | ||||
| chr9:21994169-21994706 | Common:2; Rare:172; Clinvar:17; Clinvar (benign):16; Clinvar (pathogenic):2 | ||||
| chr9:23826309-23826491 | Common:1; Rare:75 | ||||
| chr9:25678168-25678250 | Common:2; Rare:34 |