| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127916477-127916650 | Common:1; Rare:27 | ||||
| chr9:127916947-127917307 | Common:2; Rare:200 | ||||
| chr9:127928775-127929011 | Rare:50 | ||||
| chr9:127937679-127937977 | Common:4; Rare:152; Clinvar:7; Clinvar (benign):5 | ||||
| chr9:127980522-127980641 | Common:1; Rare:34 | ||||
| chr9:127980959-127981266 | Common:4; Rare:176 | ||||
| chr9:128067313-128067589 | Common:3; Rare:60 | ||||
| chr9:128067847-128068266 | Common:4; Rare:205 | ||||
| chr9:128098289-128098564 | Common:1; Rare:62 | ||||
| chr9:128122933-128123386 | Common:6; Rare:237 | ||||
| chr9:128127622-128127809 | Common:5; Rare:119 | ||||
| chr9:128128010-128128340 | Common:18; Rare:232 | ||||
| chr9:128128360-128128650 | Common:4; Rare:216 | ||||
| chr9:128149249-128149567 | Rare:116 | ||||
| chr9:128159978-128160403 | Common:6; Rare:198 |