| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:77177476-77177714 | Common:2; Rare:72; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:78031690-78032097 | Common:2; Rare:264 | ||||
| chr9:78236003-78236208 | Rare:142 | ||||
| chr9:78296828-78297261 | Common:4; Rare:198; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:81686820-81687300 | Common:2; Rare:245 | ||||
| chr9:81688670-81689220 | Common:4; Rare:273 | ||||
| chr9:81689460-81689829 | Common:20; Rare:293 | ||||
| chr9:83538234-83538501 | Common:3; Rare:154 | ||||
| chr9:83538590-83539000 | Rare:119 | ||||
| chr9:83622908-83623167 | Common:5; Rare:87 | ||||
| chr9:83707540-83708023 | Common:3; Rare:265 | ||||
| chr9:83708094-83708307 | Common:4; Rare:118 | ||||
| chr9:83817725-83818024 | Rare:219 | ||||
| chr9:83921369-83921602 | Common:4; Rare:182 | ||||
| chr9:83956474-83956817 | Common:6; Rare:191 |