| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:2621348-2621753 | Common:5; Rare:162 | ||||
| chr9:2621766-2622207 | Common:6; Rare:170; Clinvar:10; Clinvar (benign):3 | ||||
| chr9:2844034-2844372 | Common:6; Rare:133 | ||||
| chr9:3525948-3526119 | Common:1; Rare:84 | ||||
| chr9:3526420-3526521 | Common:2; Rare:53 | ||||
| chr9:4662262-4662323 | Common:1; Rare:20 | ||||
| chr9:4666409-4666536 | Rare:34 | ||||
| chr9:4679423-4679739 | Common:1; Rare:139 | ||||
| chr9:4792674-4793045 | Common:2; Rare:138 | ||||
| chr9:4984741-4985101 | Common:1; Rare:131 | ||||
| chr9:5437784-5438027 | Common:1; Rare:84 | ||||
| chr9:5450408-5450577 | Common:5; Rare:63 | ||||
| chr9:5628984-5629283 | Common:1; Rare:128 | ||||
| chr9:5890698-5890733 | Rare:6 | ||||
| chr9:5890745-5891400 | Common:2; Rare:157 |