| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:4741083-4741362 | Common:3; Rare:128 | ||||
| chr9:5628989-5629235 | Common:1; Rare:110 | ||||
| chr9:6645383-6645610 | Common:1; Rare:85; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr9:6645703-6645875 | Rare:51 | ||||
| chr9:6757876-6758169 | Common:6; Rare:117 | ||||
| chr9:13279343-13279387 | Rare:12 | ||||
| chr9:14096460-14096679 | Rare:49 | ||||
| chr9:15422709-15422895 | Rare:78 | ||||
| chr9:15552815-15553089 | Common:3; Rare:105 | ||||
| chr9:16870657-16870861 | Rare:96 | ||||
| chr9:18473944-18474223 | Rare:75 | ||||
| chr9:19049321-19049457 | Rare:63 | ||||
| chr9:19102877-19103030 | Common:1; Rare:60 | ||||
| chr9:19127420-19127581 | Common:2; Rare:49 | ||||
| chr9:19380178-19380327 | Common:4; Rare:78 |