| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7241787-7241915 | Common:1; Rare:27 | ||||
| chr17:7242269-7242590 | Common:1; Rare:105 | ||||
| chr17:7251963-7252277 | Common:1; Rare:120 | ||||
| chr17:7315075-7315406 | Common:4; Rare:116 | ||||
| chr17:7479517-7479725 | Common:1; Rare:36 | ||||
| chr17:7484207-7484371 | Common:1; Rare:67 | ||||
| chr17:7577057-7577377 | Common:1; Rare:84 | ||||
| chr17:7583542-7583865 | Common:1; Rare:132; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7584060-7584122 | Rare:18 | ||||
| chr17:7686402-7686700 | Rare:75 | ||||
| chr17:7857111-7857692 | Common:4; Rare:242 | ||||
| chr17:7885176-7885351 | Rare:57 | ||||
| chr17:7885517-7885579 | Rare:11 | ||||
| chr17:7931869-7932290 | Common:5; Rare:113 | ||||
| chr17:8176297-8176441 | Rare:52 |