| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:21214108-21214369 | Common:2; Rare:121 | ||||
| chr17:21214565-21214606 | Common:1; Rare:17 | ||||
| chr17:27293958-27294132 | Common:1; Rare:73 | ||||
| chr17:27294317-27294415 | Common:1; Rare:30 | ||||
| chr17:28318932-28319335 | Common:3; Rare:142 | ||||
| chr17:28335371-28335841 | Common:1; Rare:112 | ||||
| chr17:28357391-28357710 | Common:6; Rare:151; Clinvar (pathogenic):1 | ||||
| chr17:28370234-28370413 | Rare:25 | ||||
| chr17:28571497-28571680 | Rare:41 | ||||
| chr17:28576862-28577054 | Common:2; Rare:53 | ||||
| chr17:28598900-28599170 | Common:3; Rare:87 | ||||
| chr17:28645084-28645355 | Common:1; Rare:106 | ||||
| chr17:28661848-28661954 | Rare:47 | ||||
| chr17:28662114-28662319 | Rare:83 | ||||
| chr17:28711270-28711483 | Common:1; Rare:56 |