| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:125241286-125241713 | Common:5; Rare:137 | ||||
| chr9:125261660-125261848 | Common:2; Rare:71 | ||||
| chr9:126804869-126805070 | Common:4; Rare:65 | ||||
| chr9:126860570-126860698 | Common:2; Rare:41 | ||||
| chr9:127224396-127224652 | Rare:70 | ||||
| chr9:127245164-127245365 | Common:1; Rare:50 | ||||
| chr9:127424081-127424406 | Rare:96 | ||||
| chr9:127451267-127451565 | Common:3; Rare:123; Clinvar (benign):1 | ||||
| chr9:127612040-127612357 | Common:2; Rare:116; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:127802719-127802927 | Common:2; Rare:43 | ||||
| chr9:127927325-127927646 | Common:1; Rare:69 | ||||
| chr9:127937813-127938162 | Common:2; Rare:74; Clinvar:6; Clinvar (benign):2 | ||||
| chr9:128098212-128098539 | Common:2; Rare:67 | ||||
| chr9:128191802-128191857 | Rare:11 | ||||
| chr9:128275909-128276343 | Common:5; Rare:194 |