| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136410448-136410735 | Common:14; Rare:251; Clinvar (pathogenic):1 | ||||
| chr9:136483230-136483630 | Common:3; Rare:121 | ||||
| chr9:136483679-136483926 | Rare:131 | ||||
| chr9:136545788-136546492 | Common:6; Rare:373 | ||||
| chr9:136686880-136687290 | Common:2; Rare:155; Clinvar:2 | ||||
| chr9:136687347-136687659 | Common:4; Rare:187; Clinvar:12; Clinvar (benign):2 | ||||
| chr9:136687860-136688210 | Common:4; Rare:153 | ||||
| chr9:136791066-136791405 | Common:12; Rare:199 | ||||
| chr9:136807762-136808248 | Common:4; Rare:263 | ||||
| chr9:136823251-136823650 | Common:5; Rare:220 | ||||
| chr9:136848418-136848799 | Rare:138 | ||||
| chr9:136848810-136849050 | Common:7; Rare:138 | ||||
| chr9:136849440-136849880 | Common:2; Rare:249 | ||||
| chr9:136866192-136866520 | Common:7; Rare:237 | ||||
| chr9:136886222-136886569 | Common:4; Rare:219 |