| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:21214123-21214359 | Common:2; Rare:108 | ||||
| chr17:27293955-27294381 | Common:3; Rare:156 | ||||
| chr17:27893339-27893486 | Rare:52 | ||||
| chr17:28318912-28319243 | Common:3; Rare:115 | ||||
| chr17:28335346-28335843 | Common:1; Rare:118 | ||||
| chr17:28357355-28357699 | Common:10; Rare:161; Clinvar (pathogenic):1 | ||||
| chr17:28571497-28571732 | Rare:59 | ||||
| chr17:28576821-28577054 | Common:2; Rare:59 | ||||
| chr17:28598994-28599129 | Common:1; Rare:39 | ||||
| chr17:28645106-28645355 | Common:1; Rare:95 | ||||
| chr17:28661877-28662322 | Common:1; Rare:157 | ||||
| chr17:28719655-28720030 | Common:1; Rare:103 | ||||
| chr17:28812410-28812675 | Common:1; Rare:67 | ||||
| chr17:28842727-28842895 | Common:1; Rare:58 | ||||
| chr17:28854971-28855032 | Rare:16 |