| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44947700-44947903 | Common:1; Rare:56 | ||||
| chr17:45051453-45051688 | Common:1; Rare:84 | ||||
| chr17:45060987-45061356 | Common:2; Rare:106 | ||||
| chr17:45132340-45132657 | Common:3; Rare:95 | ||||
| chr17:45148147-45148623 | Common:1; Rare:161 | ||||
| chr17:45148947-45149235 | Common:4; Rare:80 | ||||
| chr17:45161489-45161829 | Common:1; Rare:85 | ||||
| chr17:45233806-45234090 | Common:2; Rare:57 | ||||
| chr17:45244808-45245118 | Common:1; Rare:88 | ||||
| chr17:45410349-45410513 | Rare:27 | ||||
| chr17:45431923-45432030 | Common:2; Rare:19 | ||||
| chr17:45490693-45490863 | Common:1; Rare:59 | ||||
| chr17:46193306-46193604 | Common:5; Rare:82 | ||||
| chr17:46225347-46225479 | Common:1; Rare:33 | ||||
| chr17:46922841-46923204 | Common:5; Rare:109; Clinvar:3; Clinvar (benign):8 |