| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:129718714-129718855 | Rare:24 | ||||
| chr9:130306715-130306908 | Common:1; Rare:47 | ||||
| chr9:130489109-130489379 | Common:5; Rare:59; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr9:130501795-130501879 | Common:1; Rare:17 | ||||
| chr9:130712552-130712846 | Common:6; Rare:89 | ||||
| chr9:130712970-130713118 | Rare:52 | ||||
| chr9:130817438-130817516 | Rare:10 | ||||
| chr9:131167423-131167517 | Common:1; Rare:22 | ||||
| chr9:131189072-131189254 | Rare:46 | ||||
| chr9:131281181-131281372 | Rare:39 | ||||
| chr9:131350512-131350656 | Common:4; Rare:29 | ||||
| chr9:131373383-131373706 | Common:1; Rare:75 | ||||
| chr9:131426802-131426907 | Common:1; Rare:22 | ||||
| chr9:131493280-131493400 | Rare:25 | ||||
| chr9:131770703-131770919 | Common:1; Rare:40 |