| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28371933-28372203 | Common:2; Rare:73 | ||||
| chr17:28552524-28552742 | Rare:80; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:28571466-28571727 | Rare:77 | ||||
| chr17:28571861-28571912 | Rare:10 | ||||
| chr17:28576840-28577080 | Common:2; Rare:64 | ||||
| chr17:28598736-28598777 | Rare:11 | ||||
| chr17:28598879-28599234 | Common:3; Rare:113 | ||||
| chr17:28599358-28599416 | Rare:13 | ||||
| chr17:28599469-28599779 | Rare:60 | ||||
| chr17:28645089-28645407 | Common:1; Rare:122 | ||||
| chr17:28661742-28662018 | Common:1; Rare:103 | ||||
| chr17:28662052-28662345 | Common:1; Rare:102 | ||||
| chr17:28710585-28710625 | Rare:6 | ||||
| chr17:28710931-28711096 | Common:1; Rare:32 | ||||
| chr17:28711198-28711524 | Common:3; Rare:93 |