| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:2621375-2621826 | Common:4; Rare:188; Clinvar:1 | ||||
| chr9:2621832-2622255 | Common:7; Rare:161; Clinvar:10; Clinvar (benign):6 | ||||
| chr9:2622381-2622634 | Common:2; Rare:81 | ||||
| chr9:2844043-2844347 | Common:5; Rare:115 | ||||
| chr9:3525485-3526119 | Common:2; Rare:230 | ||||
| chr9:3526409-3526719 | Common:6; Rare:147 | ||||
| chr9:4299486-4299740 | Common:1; Rare:113; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:4299860-4300267 | Common:5; Rare:161; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:4490095-4490239 | Common:2; Rare:32 | ||||
| chr9:4490321-4490554 | Common:1; Rare:78; Clinvar:3 | ||||
| chr9:4662273-4662361 | Common:1; Rare:38 | ||||
| chr9:4666317-4666490 | Common:1; Rare:38 | ||||
| chr9:4666491-4666571 | Common:1; Rare:25 | ||||
| chr9:4679423-4679834 | Common:1; Rare:180 | ||||
| chr9:4741083-4741396 | Common:6; Rare:146 |