| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133336128-133336309 | Common:1; Rare:75 | ||||
| chr9:133348037-133348274 | Common:3; Rare:97 | ||||
| chr9:133356452-133356607 | Common:1; Rare:72; Clinvar (benign):2 | ||||
| chr9:133375965-133376370 | Common:3; Rare:146 | ||||
| chr9:133417895-133418296 | Common:5; Rare:101 | ||||
| chr9:133459904-133460058 | Common:1; Rare:69 | ||||
| chr9:133738273-133738469 | Common:2; Rare:57 | ||||
| chr9:133739857-133740049 | Rare:30 | ||||
| chr9:134135282-134135403 | Common:1; Rare:23 | ||||
| chr9:134371825-134371962 | Rare:39 | ||||
| chr9:136373634-136373756 | Rare:21; Clinvar:2 | ||||
| chr9:136410431-136410680 | Common:6; Rare:110 | ||||
| chr9:136483757-136483880 | Rare:36 | ||||
| chr9:136662764-136662921 | Common:1; Rare:42 | ||||
| chr9:136849476-136849793 | Common:1; Rare:115 |