| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:19648575-19648797 | Common:3; Rare:75 | ||||
| chr17:19977804-19977934 | Common:1; Rare:42 | ||||
| chr17:21214144-21214354 | Common:2; Rare:95 | ||||
| chr17:27293911-27294122 | Common:1; Rare:87 | ||||
| chr17:28318890-28319243 | Common:3; Rare:122 | ||||
| chr17:28335387-28335834 | Common:1; Rare:106 | ||||
| chr17:28357451-28357703 | Common:5; Rare:126; Clinvar (pathogenic):1 | ||||
| chr17:28571492-28571698 | Rare:51 | ||||
| chr17:28598980-28599153 | Common:2; Rare:56 | ||||
| chr17:28645099-28645298 | Common:1; Rare:77 | ||||
| chr17:28661876-28661944 | Rare:32 | ||||
| chr17:28662166-28662319 | Rare:61 | ||||
| chr17:28717738-28717995 | Rare:55 | ||||
| chr17:28718144-28718226 | Rare:19 | ||||
| chr17:28719639-28720026 | Common:1; Rare:104 |