| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:126804922-126805069 | Common:3; Rare:46 | ||||
| chr9:127122514-127122948 | Common:4; Rare:105 | ||||
| chr9:127424073-127424464 | Common:1; Rare:113 | ||||
| chr9:127449609-127449934 | Rare:88 | ||||
| chr9:127451261-127451557 | Common:3; Rare:123; Clinvar (benign):1 | ||||
| chr9:127579021-127579305 | Common:4; Rare:59 | ||||
| chr9:127802737-127803032 | Common:3; Rare:81 | ||||
| chr9:127824889-127825142 | Rare:59; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr9:127897338-127897560 | Common:1; Rare:49 | ||||
| chr9:128098284-128098537 | Common:1; Rare:52 | ||||
| chr9:128098755-128099079 | Common:2; Rare:74 | ||||
| chr9:128190791-128191112 | Common:1; Rare:65; Clinvar:1 | ||||
| chr9:128191435-128191642 | Rare:63 | ||||
| chr9:128191755-128191861 | Common:1; Rare:25 | ||||
| chr9:128204206-128204293 | Rare:24 |