| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:132669937-132670065 | Common:1; Rare:59 | ||||
| chr9:132670304-132670537 | Rare:74 | ||||
| chr9:132878279-132878421 | Common:1; Rare:55 | ||||
| chr9:132878820-132878960 | Rare:24 | ||||
| chr9:133030445-133030791 | Common:4; Rare:100 | ||||
| chr9:133054413-133055048 | Common:2; Rare:193 | ||||
| chr9:133336047-133336239 | Common:1; Rare:97 | ||||
| chr9:133347925-133348335 | Common:4; Rare:148 | ||||
| chr9:133356399-133356619 | Common:1; Rare:105; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr9:133375925-133376442 | Common:5; Rare:182 | ||||
| chr9:133417952-133418352 | Common:4; Rare:97 | ||||
| chr9:133459963-133460051 | Common:1; Rare:42 | ||||
| chr9:134135952-134136127 | Common:2; Rare:62 | ||||
| chr9:134641551-134642004 | Common:2; Rare:125; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:134642125-134642291 | Common:4; Rare:51; Clinvar:7; Clinvar (benign):7 |