| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:27456177-27456556 | Common:2; Rare:118 | ||||
| chr17:27471681-27471994 | Rare:55 | ||||
| chr17:27631073-27631267 | Rare:65 | ||||
| chr17:27631356-27631462 | Rare:13 | ||||
| chr17:27631548-27631666 | Rare:32 | ||||
| chr17:27893176-27893511 | Common:2; Rare:108 | ||||
| chr17:28041484-28041823 | Common:2; Rare:87 | ||||
| chr17:28318822-28319317 | Common:3; Rare:180 | ||||
| chr17:28319319-28319450 | Common:4; Rare:44 | ||||
| chr17:28335389-28335849 | Common:1; Rare:108 | ||||
| chr17:28336159-28336256 | Common:2; Rare:21 | ||||
| chr17:28357406-28357767 | Common:6; Rare:174; Clinvar (pathogenic):2 | ||||
| chr17:28371461-28372024 | Common:5; Rare:102 | ||||
| chr17:28384431-28384921 | Rare:142 | ||||
| chr17:28385142-28385237 | Rare:36 |