| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127980953-127981253 | Common:4; Rare:167 | ||||
| chr9:128067892-128068251 | Common:2; Rare:95 | ||||
| chr9:128098257-128098553 | Common:2; Rare:64 | ||||
| chr9:128122818-128123399 | Common:8; Rare:308 | ||||
| chr9:128127636-128127809 | Common:5; Rare:111 | ||||
| chr9:128128067-128128315 | Common:18; Rare:203 | ||||
| chr9:128128363-128128524 | Common:4; Rare:137 | ||||
| chr9:128159940-128160405 | Common:5; Rare:193 | ||||
| chr9:128191482-128191703 | Common:1; Rare:101 | ||||
| chr9:128191727-128191848 | Common:2; Rare:53 | ||||
| chr9:128250413-128250728 | Rare:76; Clinvar (benign):1 | ||||
| chr9:128275907-128276340 | Common:10; Rare:382 | ||||
| chr9:128322399-128322637 | Common:2; Rare:135 | ||||
| chr9:128322718-128322910 | Common:4; Rare:179; Clinvar:6; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
| chr9:128340417-128340579 | Common:2; Rare:103 |