| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:37576209-37576430 | Rare:56 | ||||
| chr9:37592478-37592671 | Common:2; Rare:69 | ||||
| chr9:37784864-37785149 | Common:1; Rare:128; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr9:37800635-37800829 | Common:2; Rare:69 | ||||
| chr9:37904059-37904211 | Rare:52 | ||||
| chr9:37904308-37904461 | Rare:58 | ||||
| chr9:38424451-38424588 | Rare:39 | ||||
| chr9:66900574-66900814 | Common:3; Rare:76 | ||||
| chr9:68779694-68780165 | Common:6; Rare:136 | ||||
| chr9:69672255-69672570 | Common:1; Rare:89 | ||||
| chr9:69759924-69760099 | Common:2; Rare:85 | ||||
| chr9:70258823-70259075 | Common:4; Rare:119 | ||||
| chr9:71768497-71768602 | Rare:26 | ||||
| chr9:71911168-71911508 | Common:3; Rare:100 | ||||
| chr9:72363973-72364036 | Rare:12 |