| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:2621837-2622169 | Common:4; Rare:112; Clinvar:7; Clinvar (benign):2 | ||||
| chr9:2844043-2844357 | Common:5; Rare:124 | ||||
| chr9:3525500-3525617 | Rare:54 | ||||
| chr9:3525763-3526119 | Common:1; Rare:133 | ||||
| chr9:4490343-4490670 | Common:1; Rare:111; Clinvar:5 | ||||
| chr9:4662178-4662297 | Common:3; Rare:44 | ||||
| chr9:4666388-4666569 | Common:2; Rare:52 | ||||
| chr9:4679437-4679846 | Common:1; Rare:179 | ||||
| chr9:4792674-4792996 | Common:2; Rare:124 | ||||
| chr9:4984868-4985102 | Common:1; Rare:70 | ||||
| chr9:5437791-5437995 | Common:1; Rare:72 | ||||
| chr9:5628894-5629224 | Common:1; Rare:163 | ||||
| chr9:6015576-6015719 | Rare:64 | ||||
| chr9:6645703-6645900 | Rare:64 | ||||
| chr9:6757865-6758141 | Common:5; Rare:111 |