| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:18473941-18474154 | Rare:55 | ||||
| chr9:19049705-19050180 | Common:2; Rare:89 | ||||
| chr9:20684060-20684288 | Common:3; Rare:92 | ||||
| chr9:21994186-21994514 | Rare:121; Clinvar:16; Clinvar (benign):15; Clinvar (pathogenic):2 | ||||
| chr9:26892347-26892449 | Rare:43 | ||||
| chr9:33025098-33025297 | Common:5; Rare:79 | ||||
| chr9:33264641-33265102 | Common:1; Rare:133 | ||||
| chr9:34126369-34126457 | Rare:34 | ||||
| chr9:34178973-34179072 | Common:1; Rare:30 | ||||
| chr9:34329213-34329588 | Rare:114 | ||||
| chr9:35732115-35732683 | Common:4; Rare:158 | ||||
| chr9:35748867-35749316 | Common:3; Rare:135 | ||||
| chr9:37800705-37800903 | Common:1; Rare:66 | ||||
| chr9:37904084-37904450 | Common:3; Rare:117 | ||||
| chr9:71911018-71911514 | Common:3; Rare:144 |