| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:22523302-22523422 | Rare:27 | ||||
| chr17:27293919-27294196 | Common:2; Rare:109 | ||||
| chr17:27294318-27294682 | Common:3; Rare:99 | ||||
| chr17:27559792-27560164 | Common:1; Rare:76 | ||||
| chr17:27577127-27577352 | Common:1; Rare:46 | ||||
| chr17:27592391-27592580 | Common:1; Rare:55 | ||||
| chr17:28042213-28042641 | Common:2; Rare:97 | ||||
| chr17:28318937-28319257 | Common:3; Rare:115 | ||||
| chr17:28329219-28329319 | Rare:32 | ||||
| chr17:28331858-28332198 | Common:1; Rare:91 | ||||
| chr17:28335342-28335849 | Common:1; Rare:121 | ||||
| chr17:28357370-28357695 | Common:6; Rare:153; Clinvar (pathogenic):1 | ||||
| chr17:28372443-28372745 | Rare:69 | ||||
| chr17:28598917-28599136 | Common:2; Rare:73 | ||||
| chr17:28645059-28645337 | Common:1; Rare:115 |