| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:32525392-32525641 | Common:1; Rare:42 | ||||
| chr9:32550829-32551353 | Common:2; Rare:171; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:32551390-32551507 | Rare:33 | ||||
| chr9:33044448-33044582 | Common:2; Rare:48 | ||||
| chr9:33129886-33130030 | Rare:36 | ||||
| chr9:33136838-33136913 | Common:1; Rare:22 | ||||
| chr9:33161141-33161348 | Rare:31 | ||||
| chr9:33165832-33166045 | Common:1; Rare:41 | ||||
| chr9:33166481-33166586 | Rare:25 | ||||
| chr9:33202665-33202799 | Rare:22 | ||||
| chr9:33446418-33446770 | Common:2; Rare:62 | ||||
| chr9:33458462-33458490 | Rare:3 | ||||
| chr9:33809089-33809299 | Common:1; Rare:31 | ||||
| chr9:33816636-33816818 | Common:1; Rare:41 | ||||
| chr9:33818278-33818489 | Common:2; Rare:36 |