| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128881909-128882197 | Common:2; Rare:95 | ||||
| chr9:128947573-128947749 | Common:2; Rare:82; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:129110661-129110962 | Common:4; Rare:68 | ||||
| chr9:129111264-129111607 | Common:3; Rare:95 | ||||
| chr9:129139935-129140129 | Rare:40 | ||||
| chr9:129141936-129142028 | Common:3; Rare:21 | ||||
| chr9:129642130-129642433 | Common:2; Rare:70 | ||||
| chr9:129752943-129753165 | Common:2; Rare:72 | ||||
| chr9:129824087-129824318 | Common:4; Rare:62; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:129835159-129835487 | Common:3; Rare:130 | ||||
| chr9:130043052-130043293 | Common:2; Rare:74 | ||||
| chr9:130053580-130053741 | Rare:35 | ||||
| chr9:130053840-130054041 | Common:1; Rare:77 | ||||
| chr9:130579442-130579754 | Common:7; Rare:117 | ||||
| chr9:130693592-130693846 | Common:1; Rare:97 |