| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:19376301-19376509 | Common:2; Rare:78 | ||||
| chr9:19380205-19380334 | Common:4; Rare:63 | ||||
| chr9:21031577-21031737 | Common:1; Rare:64 | ||||
| chr9:21994222-21994797 | Common:2; Rare:177; Clinvar:13; Clinvar (benign):13; Clinvar (pathogenic):2 | ||||
| chr9:21994921-21995095 | Common:1; Rare:28 | ||||
| chr9:26947146-26947271 | Rare:44 | ||||
| chr9:33025093-33025304 | Common:5; Rare:89 | ||||
| chr9:33076598-33076793 | Common:2; Rare:71 | ||||
| chr9:33264696-33265123 | Rare:118 | ||||
| chr9:34048873-34048992 | Common:1; Rare:46 | ||||
| chr9:34329238-34329539 | Rare:88 | ||||
| chr9:34637725-34638134 | Common:3; Rare:106 | ||||
| chr9:34652039-34652222 | Rare:55 | ||||
| chr9:35685270-35685469 | Rare:47; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:35732083-35732683 | Common:5; Rare:168 |