| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:73151700-73151924 | Common:1; Rare:41 | ||||
| chr9:74952207-74952414 | Rare:66 | ||||
| chr9:74952835-74953004 | Common:1; Rare:45 | ||||
| chr9:75027772-75027958 | Rare:49 | ||||
| chr9:75088099-75088563 | Common:4; Rare:160 | ||||
| chr9:75890513-75890683 | Common:2; Rare:49 | ||||
| chr9:76393752-76393893 | Common:1; Rare:35 | ||||
| chr9:76393941-76394062 | Common:1; Rare:41 | ||||
| chr9:76394100-76394181 | Rare:23 | ||||
| chr9:76394187-76394614 | Common:9; Rare:156 | ||||
| chr9:76459064-76459239 | Common:1; Rare:62 | ||||
| chr9:77177468-77177714 | Common:2; Rare:75; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:78235984-78236165 | Rare:65 | ||||
| chr9:78296822-78297247 | Common:2; Rare:116; Clinvar (benign):1 | ||||
| chr9:81689464-81689816 | Common:10; Rare:147 |