| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42609863-42610267 | Rare:231; Clinvar (benign):2 | ||||
| chr17:42610335-42610735 | Common:1; Rare:86 | ||||
| chr17:42660695-42661095 | Common:2; Rare:77 | ||||
| chr17:42673795-42674728 | Common:5; Rare:357 | ||||
| chr17:42676469-42676869 | Common:1; Rare:103 | ||||
| chr17:42676919-42677431 | Common:6; Rare:623 | ||||
| chr17:42681152-42681562 | Common:9; Rare:122 | ||||
| chr17:42744549-42745278 | Common:12; Rare:514 | ||||
| chr17:42773262-42773912 | Rare:469 | ||||
| chr17:42773878-42774086 | Common:2; Rare:62 | ||||
| chr17:42779940-42780732 | Common:26; Rare:766; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:42781046-42781555 | Common:2; Rare:169; Clinvar (benign):2 | ||||
| chr17:42798490-42799050 | Common:1; Rare:467 | ||||
| chr17:42824112-42824651 | Common:16; Rare:638 | ||||
| chr17:42832409-42832911 | Common:2; Rare:118 |