| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:352966-353277 | Common:5; Rare:59 | ||||
| chr17:386209-386459 | Common:3; Rare:55 | ||||
| chr17:714782-714915 | Common:2; Rare:45 | ||||
| chr17:732311-732698 | Common:2; Rare:135 | ||||
| chr17:752146-752360 | Common:2; Rare:84 | ||||
| chr17:996787-997190 | Common:2; Rare:133 | ||||
| chr17:1115388-1115643 | Common:1; Rare:50 | ||||
| chr17:1400046-1400373 | Common:3; Rare:135 | ||||
| chr17:1400378-1400413 | Rare:9 | ||||
| chr17:1485720-1486051 | Common:3; Rare:112 | ||||
| chr17:1491202-1491306 | Common:1; Rare:22 | ||||
| chr17:1516582-1516984 | Common:2; Rare:143 | ||||
| chr17:1684798-1685008 | Common:1; Rare:70; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:1716175-1716541 | Common:3; Rare:114 | ||||
| chr17:1717092-1717304 | Common:1; Rare:51 |