| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:19127467-19127574 | Common:1; Rare:29 | ||||
| chr9:19380092-19380377 | Common:6; Rare:133 | ||||
| chr9:20622446-20622718 | Common:1; Rare:88 | ||||
| chr9:20684078-20684283 | Common:3; Rare:80 | ||||
| chr9:21802540-21802751 | Common:1; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:23826303-23826510 | Common:1; Rare:82 | ||||
| chr9:26892338-26892479 | Rare:63 | ||||
| chr9:26892719-26892895 | Common:1; Rare:85 | ||||
| chr9:26947107-26947305 | Common:1; Rare:70 | ||||
| chr9:26947444-26947577 | Common:1; Rare:36 | ||||
| chr9:26956302-26956499 | Common:2; Rare:73 | ||||
| chr9:27573709-27573944 | Common:2; Rare:75; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:32551995-32552368 | Common:2; Rare:100 | ||||
| chr9:32552541-32552633 | Common:1; Rare:17; Clinvar:2 | ||||
| chr9:32573051-32573229 | Common:3; Rare:63 |