| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:129803047-129803229 | Common:4; Rare:135 | ||||
| chr9:129824087-129824299 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:129835112-129835510 | Common:7; Rare:256 | ||||
| chr9:130053480-130053983 | Common:3; Rare:215 | ||||
| chr9:130172253-130172574 | Common:4; Rare:164 | ||||
| chr9:130444726-130444993 | Common:2; Rare:149; Clinvar:16; Clinvar (benign):2 | ||||
| chr9:130445283-130445485 | Common:1; Rare:30 | ||||
| chr9:130578830-130579118 | Common:4; Rare:102 | ||||
| chr9:130579424-130579754 | Common:14; Rare:229 | ||||
| chr9:130693578-130693890 | Common:1; Rare:194; Clinvar (pathogenic):1 | ||||
| chr9:130713590-130713910 | Common:2; Rare:138 | ||||
| chr9:130834709-130835373 | Common:13; Rare:264 | ||||
| chr9:130939153-130939314 | Common:4; Rare:48 | ||||
| chr9:131096335-131096561 | Common:3; Rare:60 | ||||
| chr9:131125362-131125744 | Common:5; Rare:299 |