| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35103090-35103309 | Common:1; Rare:71 | ||||
| chr9:35162288-35162384 | Rare:28 | ||||
| chr9:35489757-35490154 | Common:3; Rare:123 | ||||
| chr9:35563870-35564176 | Common:1; Rare:83 | ||||
| chr9:35657850-35658496 | Common:10; Rare:479; Clinvar:42; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35685420-35685637 | Common:1; Rare:50; Clinvar (benign):2 | ||||
| chr9:35689681-35690123 | Common:4; Rare:136; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35705961-35706367 | Common:3; Rare:91 | ||||
| chr9:35732074-35732334 | Common:2; Rare:70 | ||||
| chr9:35732365-35732684 | Common:3; Rare:82 | ||||
| chr9:35748756-35748770 | Rare:2 | ||||
| chr9:35748993-35749397 | Common:2; Rare:150 | ||||
| chr9:35812242-35812278 | Rare:13 | ||||
| chr9:35815040-35815293 | Rare:59 | ||||
| chr9:35906106-35906267 | Rare:37 |