| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:215016-215208 | Common:5; Rare:117; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:215728-216007 | Common:1; Rare:66 | ||||
| chr9:470117-470404 | Common:16; Rare:129 | ||||
| chr9:504391-504738 | Common:4; Rare:169 | ||||
| chr9:2017492-2017699 | Rare:60 | ||||
| chr9:2844047-2844357 | Common:5; Rare:122 | ||||
| chr9:3525751-3526119 | Common:1; Rare:134 | ||||
| chr9:3526421-3526512 | Common:2; Rare:47 | ||||
| chr9:4490104-4490216 | Common:2; Rare:20 | ||||
| chr9:4679437-4679775 | Common:1; Rare:148 | ||||
| chr9:4741083-4741400 | Common:6; Rare:149 | ||||
| chr9:4741753-4741955 | Common:4; Rare:67 | ||||
| chr9:5437803-5437982 | Common:1; Rare:65 | ||||
| chr9:6015591-6015741 | Rare:70 | ||||
| chr9:6645700-6645875 | Rare:51 |