| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92877969-92878203 | Common:2; Rare:69 | ||||
| chr9:93134218-93134361 | Common:2; Rare:49 | ||||
| chr9:93451472-93451717 | Common:3; Rare:76 | ||||
| chr9:93452291-93452324 | Rare:4 | ||||
| chr9:93453546-93453687 | Rare:31 | ||||
| chr9:94259290-94259338 | Rare:15 | ||||
| chr9:94726547-94726745 | Rare:57 | ||||
| chr9:95048376-95048624 | Rare:59 | ||||
| chr9:95317681-95317816 | Common:1; Rare:39; Clinvar:1 | ||||
| chr9:95505863-95506188 | Common:1; Rare:114 | ||||
| chr9:95506597-95506691 | Common:1; Rare:38; Clinvar (benign):3 | ||||
| chr9:95875432-95875750 | Common:1; Rare:114 | ||||
| chr9:95875961-95876084 | Common:5; Rare:62; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:96383483-96383783 | Common:3; Rare:100 | ||||
| chr9:96654868-96654907 | Rare:12 |