| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28661839-28661952 | Rare:101 | ||||
| chr17:28662107-28662319 | Rare:87 | ||||
| chr17:28674360-28674640 | Rare:105 | ||||
| chr17:28711263-28711477 | Common:2; Rare:106 | ||||
| chr17:28719655-28720054 | Common:1; Rare:177 | ||||
| chr17:28725668-28725928 | Common:2; Rare:146 | ||||
| chr17:28726162-28726349 | Common:6; Rare:79 | ||||
| chr17:28727190-28727490 | Rare:94 | ||||
| chr17:28727925-28728080 | Rare:59 | ||||
| chr17:28728546-28728946 | Rare:178; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:28743657-28744158 | Common:8; Rare:185 | ||||
| chr17:28812359-28812674 | Common:2; Rare:133 | ||||
| chr17:28842717-28842908 | Common:4; Rare:129 | ||||
| chr17:28854661-28855093 | Common:2; Rare:133 | ||||
| chr17:28897590-28897739 | Common:2; Rare:100 |