| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128881821-128882206 | Common:4; Rare:211 | ||||
| chr9:128882370-128882700 | Common:3; Rare:134 | ||||
| chr9:128947526-128947835 | Common:3; Rare:223; Clinvar:12; Clinvar (benign):3 | ||||
| chr9:129028169-129028612 | Common:10; Rare:268 | ||||
| chr9:129036330-129036684 | Common:5; Rare:180 | ||||
| chr9:129080884-129081144 | Common:2; Rare:75 | ||||
| chr9:129081200-129081600 | Common:1; Rare:155 | ||||
| chr9:129110670-129110979 | Common:8; Rare:129 | ||||
| chr9:129111291-129111439 | Common:4; Rare:102 | ||||
| chr9:129139904-129140246 | Rare:158 | ||||
| chr9:129178185-129178455 | Common:5; Rare:179 | ||||
| chr9:129626091-129626199 | Rare:37 | ||||
| chr9:129626310-129626560 | Common:4; Rare:77 | ||||
| chr9:129642061-129642467 | Common:6; Rare:153 | ||||
| chr9:129752888-129753181 | Common:4; Rare:185 |