| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127899518-127899752 | Common:1; Rare:84 | ||||
| chr9:127937824-127937878 | Common:1; Rare:20; Clinvar (benign):1 | ||||
| chr9:128098291-128098537 | Common:1; Rare:51 | ||||
| chr9:128160008-128160464 | Common:2; Rare:109 | ||||
| chr9:128191748-128191936 | Common:1; Rare:53 | ||||
| chr9:128275909-128276307 | Common:5; Rare:173 | ||||
| chr9:128322410-128322576 | Common:1; Rare:54 | ||||
| chr9:128322739-128322870 | Common:2; Rare:52; Clinvar (benign):5 | ||||
| chr9:128340419-128340691 | Common:2; Rare:87 | ||||
| chr9:128371193-128371398 | Rare:76 | ||||
| chr9:128428764-128428955 | Rare:78 | ||||
| chr9:128455917-128456208 | Common:2; Rare:100 | ||||
| chr9:128504598-128504782 | Rare:85; Clinvar:5 | ||||
| chr9:128552408-128552597 | Rare:73; Clinvar:1 | ||||
| chr9:128656644-128656816 | Common:2; Rare:77; Clinvar (pathogenic):1 |