| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:130579442-130579677 | Common:7; Rare:94 | ||||
| chr9:132878282-132878408 | Common:1; Rare:47 | ||||
| chr9:133336146-133336354 | Common:1; Rare:82 | ||||
| chr9:133348039-133348237 | Common:2; Rare:72 | ||||
| chr9:133356380-133356607 | Common:2; Rare:101; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr9:133375947-133376277 | Common:2; Rare:117 | ||||
| chr9:133417953-133418293 | Common:4; Rare:80 | ||||
| chr9:136118817-136119045 | Common:4; Rare:98 | ||||
| chr9:136410447-136410666 | Common:6; Rare:100 | ||||
| chr9:136807770-136807933 | Common:1; Rare:70 | ||||
| chr9:136849345-136849770 | Common:3; Rare:183 | ||||
| chr9:137086658-137087002 | Common:1; Rare:132; Clinvar:1 | ||||
| chr9:137188547-137188717 | Common:2; Rare:85 | ||||
| chr9:137200738-137201053 | Common:3; Rare:86 | ||||
| chr9:137205567-137205741 | Rare:69 |