| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:339023-339137 | Common:1; Rare:23 | ||||
| chr17:352532-352634 | Common:1; Rare:25 | ||||
| chr17:352735-352867 | Common:1; Rare:33 | ||||
| chr17:386209-386443 | Common:3; Rare:51 | ||||
| chr17:714777-714899 | Common:2; Rare:40 | ||||
| chr17:1400048-1400340 | Common:2; Rare:122 | ||||
| chr17:1455920-1456029 | Rare:27 | ||||
| chr17:1491605-1491816 | Common:1; Rare:63 | ||||
| chr17:1516588-1516981 | Common:2; Rare:138 | ||||
| chr17:1661740-1662036 | Common:2; Rare:70; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:1673161-1673413 | Common:2; Rare:60; Clinvar:1 | ||||
| chr17:1679193-1679312 | Rare:36; Clinvar:1 | ||||
| chr17:1684794-1685038 | Common:2; Rare:80; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:1716172-1716448 | Common:1; Rare:92 | ||||
| chr17:1717061-1717339 | Common:1; Rare:63 |