| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:27293899-27294134 | Common:1; Rare:94 | ||||
| chr17:27294539-27294644 | Common:1; Rare:26 | ||||
| chr17:27456201-27456487 | Common:1; Rare:91 | ||||
| chr17:27893152-27893495 | Common:2; Rare:110 | ||||
| chr17:28041014-28041760 | Common:7; Rare:221 | ||||
| chr17:28318884-28319235 | Common:3; Rare:119 | ||||
| chr17:28335411-28335817 | Common:1; Rare:92 | ||||
| chr17:28336151-28336493 | Common:2; Rare:62 | ||||
| chr17:28357465-28357708 | Common:5; Rare:121; Clinvar (pathogenic):1 | ||||
| chr17:28370246-28370475 | Common:1; Rare:31 | ||||
| chr17:28371343-28371570 | Common:2; Rare:43 | ||||
| chr17:28406010-28406430 | Common:1; Rare:105; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr17:28551910-28552800 | Common:2; Rare:265; Clinvar:6; Clinvar (benign):2 | ||||
| chr17:28570723-28571123 | Rare:163; Clinvar (pathogenic):1 | ||||
| chr17:28571450-28571990 | Common:1; Rare:141 |