| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:14307998-14308304 | Common:1; Rare:63 | ||||
| chr9:14314506-14314816 | Common:3; Rare:72 | ||||
| chr9:14693244-14693376 | Common:1; Rare:55 | ||||
| chr9:15422630-15422921 | Common:1; Rare:135 | ||||
| chr9:15552774-15553201 | Common:4; Rare:161 | ||||
| chr9:17134965-17135062 | Rare:45 | ||||
| chr9:19102850-19103067 | Common:2; Rare:93 | ||||
| chr9:19230302-19230649 | Common:6; Rare:134 | ||||
| chr9:19380188-19380360 | Common:4; Rare:84 | ||||
| chr9:20621831-20622077 | Common:3; Rare:76 | ||||
| chr9:20622384-20622728 | Common:2; Rare:117 | ||||
| chr9:20658236-20658429 | Common:5; Rare:89 | ||||
| chr9:20684096-20684292 | Common:3; Rare:80 | ||||
| chr9:21802540-21802677 | Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:23826077-23826493 | Common:2; Rare:151 |