| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:178952-179221 | Common:4; Rare:52 | ||||
| chr9:214717-214889 | Common:3; Rare:95; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:215081-215220 | Common:2; Rare:77 | ||||
| chr9:504391-504730 | Common:4; Rare:166 | ||||
| chr9:706853-707187 | Common:3; Rare:111 | ||||
| chr9:2015048-2015387 | Common:3; Rare:100 | ||||
| chr9:2016964-2017188 | Rare:56 | ||||
| chr9:2017476-2017736 | Rare:78 | ||||
| chr9:2844034-2844352 | Common:5; Rare:122 | ||||
| chr9:3525751-3526106 | Common:1; Rare:122 | ||||
| chr9:3526402-3526540 | Common:4; Rare:72 | ||||
| chr9:4299941-4300267 | Common:5; Rare:125; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:4490108-4490222 | Common:2; Rare:21 | ||||
| chr9:4662262-4662323 | Common:1; Rare:20 | ||||
| chr9:4679423-4679830 | Common:1; Rare:179 |