| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44557020-44557485 | Common:5; Rare:222 | ||||
| chr17:44689664-44689906 | Rare:102 | ||||
| chr17:44708498-44708770 | Common:2; Rare:95 | ||||
| chr17:44774880-44775282 | Common:4; Rare:103 | ||||
| chr17:44775620-44776024 | Common:10; Rare:183 | ||||
| chr17:44899337-44899801 | Common:8; Rare:382; Clinvar:8; Clinvar (benign):3 | ||||
| chr17:44947584-44948015 | Common:3; Rare:263 | ||||
| chr17:44968263-44968580 | Rare:235 | ||||
| chr17:45051302-45052134 | Common:25; Rare:502 | ||||
| chr17:45060163-45060778 | Common:6; Rare:204 | ||||
| chr17:45060922-45061461 | Common:5; Rare:394 | ||||
| chr17:45102576-45102919 | Rare:129 | ||||
| chr17:45132360-45132768 | Common:8; Rare:286 | ||||
| chr17:45133201-45133343 | Rare:23 | ||||
| chr17:45148141-45148679 | Common:2; Rare:343 |