| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:27573437-27573524 | Common:5; Rare:47 | ||||
| chr9:32384524-32384728 | Common:1; Rare:79 | ||||
| chr9:32573052-32573219 | Common:2; Rare:62 | ||||
| chr9:33025035-33025383 | Common:7; Rare:141 | ||||
| chr9:33076583-33076812 | Common:2; Rare:75 | ||||
| chr9:33166826-33166966 | Rare:51; Clinvar:1 | ||||
| chr9:33290261-33290570 | Common:3; Rare:106 | ||||
| chr9:33290867-33290957 | Rare:22 | ||||
| chr9:33473857-33474153 | Common:3; Rare:89 | ||||
| chr9:34048870-34048960 | Rare:36 | ||||
| chr9:34329213-34329593 | Rare:118 | ||||
| chr9:34665373-34665678 | Rare:99 | ||||
| chr9:35103078-35103196 | Common:1; Rare:46 | ||||
| chr9:35489778-35490148 | Common:3; Rare:117 | ||||
| chr9:35657841-35658376 | Common:9; Rare:443; Clinvar:42; Clinvar (benign):16; Clinvar (pathogenic):40 |