| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97633719-97633829 | Common:2; Rare:34 | ||||
| chr9:100098989-100099260 | Common:1; Rare:69 | ||||
| chr9:101398594-101398887 | Common:1; Rare:95 | ||||
| chr9:113221294-113221584 | Rare:89 | ||||
| chr9:113275403-113275689 | Common:4; Rare:83; Clinvar (pathogenic):1 | ||||
| chr9:122264762-122264894 | Common:2; Rare:41 | ||||
| chr9:127451329-127451527 | Common:2; Rare:86 | ||||
| chr9:128275939-128276288 | Common:4; Rare:163 | ||||
| chr9:128371225-128371375 | Rare:47 | ||||
| chr9:128552433-128552611 | Rare:74; Clinvar:1 | ||||
| chr9:128724102-128724229 | Common:1; Rare:44 | ||||
| chr9:128947604-128947716 | Common:1; Rare:51; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129835225-129835452 | Common:2; Rare:94 | ||||
| chr9:133348087-133348246 | Common:1; Rare:63 | ||||
| chr9:133376007-133376366 | Common:1; Rare:131 |