| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133163912-133164036 | Common:3; Rare:29 | ||||
| chr9:133348048-133348268 | Common:2; Rare:90 | ||||
| chr9:133356431-133356595 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:133375973-133376367 | Common:3; Rare:143 | ||||
| chr9:133417953-133418294 | Common:4; Rare:80 | ||||
| chr9:134641551-134641904 | Common:2; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:136118816-136119043 | Common:4; Rare:97 | ||||
| chr9:136327330-136327616 | Common:4; Rare:103 | ||||
| chr9:136410460-136410689 | Common:7; Rare:110 | ||||
| chr9:136807809-136807949 | Common:1; Rare:56 | ||||
| chr9:136849620-136849760 | Common:1; Rare:55 | ||||
| chr9:136944604-136944912 | Common:2; Rare:117 | ||||
| chr9:137086629-137087139 | Common:2; Rare:212; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:137188534-137188727 | Common:2; Rare:95 | ||||
| chr9:137204499-137204561 | Rare:14 |