| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42017367-42017533 | Common:1; Rare:68 | ||||
| chr17:42017555-42017711 | Rare:44 | ||||
| chr17:42154894-42155208 | Common:3; Rare:83 | ||||
| chr17:42458738-42458953 | Common:3; Rare:81 | ||||
| chr17:42566940-42567159 | Common:3; Rare:77 | ||||
| chr17:42577651-42577896 | Common:1; Rare:126 | ||||
| chr17:42586951-42587092 | Rare:26 | ||||
| chr17:42609328-42609732 | Common:8; Rare:170; Clinvar (benign):2 | ||||
| chr17:42675989-42676159 | Rare:35 | ||||
| chr17:42676955-42677242 | Common:1; Rare:80 | ||||
| chr17:42745023-42745172 | Common:3; Rare:54 | ||||
| chr17:42761075-42761263 | Rare:52 | ||||
| chr17:42773375-42773508 | Rare:42 | ||||
| chr17:42798632-42798785 | Rare:50 | ||||
| chr17:42833351-42833491 | Rare:54 |