| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:21214118-21214361 | Common:2; Rare:114 | ||||
| chr17:21253233-21253322 | Common:1; Rare:31 | ||||
| chr17:27293948-27294186 | Common:2; Rare:97 | ||||
| chr17:27294310-27294435 | Common:1; Rare:35 | ||||
| chr17:28042250-28042633 | Common:2; Rare:85 | ||||
| chr17:28318937-28319251 | Common:3; Rare:111 | ||||
| chr17:28335376-28335841 | Common:1; Rare:112 | ||||
| chr17:28357396-28357744 | Common:6; Rare:164; Clinvar (pathogenic):1 | ||||
| chr17:28371219-28371762 | Common:6; Rare:105 | ||||
| chr17:28552550-28552744 | Rare:73; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:28571497-28571716 | Rare:53 | ||||
| chr17:28599007-28599127 | Common:1; Rare:31 | ||||
| chr17:28645076-28645289 | Common:1; Rare:84 | ||||
| chr17:28661876-28661957 | Rare:37 | ||||
| chr17:28662093-28662337 | Rare:94 |