| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127762408-127762654 | Common:2; Rare:60 | ||||
| chr9:127802753-127802989 | Common:3; Rare:61 | ||||
| chr9:127937824-127937968 | Common:1; Rare:37; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:128160008-128160449 | Common:2; Rare:104 | ||||
| chr9:128191499-128191651 | Rare:44 | ||||
| chr9:128191748-128191863 | Common:1; Rare:29 | ||||
| chr9:128275914-128276302 | Common:5; Rare:172 | ||||
| chr9:128322404-128322576 | Common:1; Rare:57 | ||||
| chr9:128322739-128322870 | Common:2; Rare:52; Clinvar (benign):5 | ||||
| chr9:128371204-128371399 | Rare:73 | ||||
| chr9:128552408-128552622 | Rare:86; Clinvar:1 | ||||
| chr9:128724070-128724464 | Common:2; Rare:133 | ||||
| chr9:128771854-128771987 | Rare:40 | ||||
| chr9:128787148-128787341 | Common:3; Rare:65 | ||||
| chr9:128881907-128882206 | Common:2; Rare:100 |