| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128881901-128882192 | Common:1; Rare:94 | ||||
| chr9:128947598-128947716 | Common:1; Rare:54; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129111242-129111573 | Common:2; Rare:98 | ||||
| chr9:129835210-129835492 | Common:2; Rare:114 | ||||
| chr9:130043053-130043321 | Common:2; Rare:88 | ||||
| chr9:130053871-130053959 | Common:1; Rare:36 | ||||
| chr9:130693626-130693791 | Rare:53 | ||||
| chr9:131125417-131125651 | Common:2; Rare:111 | ||||
| chr9:131502866-131503033 | Rare:58; Clinvar:3 | ||||
| chr9:131531182-131531357 | Common:9; Rare:80 | ||||
| chr9:132354955-132355208 | Common:3; Rare:81 | ||||
| chr9:132669948-132670040 | Common:1; Rare:45 | ||||
| chr9:132878272-132878360 | Common:1; Rare:30 | ||||
| chr9:133163912-133164047 | Common:3; Rare:33 | ||||
| chr9:133336133-133336290 | Common:1; Rare:60 |