| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35489640-35489890 | Rare:71 | ||||
| chr9:35489921-35490152 | Common:3; Rare:65 | ||||
| chr9:35538394-35538650 | Common:1; Rare:38 | ||||
| chr9:35538700-35538920 | Common:1; Rare:49 | ||||
| chr9:35539070-35539360 | Common:1; Rare:53 | ||||
| chr9:35646746-35647024 | Common:2; Rare:65 | ||||
| chr9:35657927-35658429 | Common:8; Rare:381; Clinvar:26; Clinvar (benign):13; Clinvar (pathogenic):36 | ||||
| chr9:35658546-35658714 | Rare:62 | ||||
| chr9:35665156-35665451 | Common:3; Rare:95 | ||||
| chr9:35690866-35691040 | Common:1; Rare:42 | ||||
| chr9:35691060-35691258 | Common:1; Rare:41 | ||||
| chr9:35731941-35732356 | Common:2; Rare:114 | ||||
| chr9:35732368-35732676 | Common:2; Rare:77 | ||||
| chr9:35749040-35749490 | Common:2; Rare:167 | ||||
| chr9:35756538-35756983 | Common:6; Rare:129 |