| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:20009255-20009399 | Common:3; Rare:44 | ||||
| chr17:20896161-20896231 | Common:1; Rare:38 | ||||
| chr17:21019144-21019448 | Common:1; Rare:62 | ||||
| chr17:21042220-21042394 | Common:1; Rare:68 | ||||
| chr17:21214108-21214355 | Common:2; Rare:113 | ||||
| chr17:21214565-21214618 | Common:1; Rare:22 | ||||
| chr17:21253247-21253543 | Common:3; Rare:95 | ||||
| chr17:27294007-27294180 | Common:2; Rare:68 | ||||
| chr17:27294276-27294384 | Common:1; Rare:31 | ||||
| chr17:28335363-28335841 | Common:1; Rare:114 | ||||
| chr17:28357353-28357692 | Common:10; Rare:159; Clinvar (pathogenic):1 | ||||
| chr17:28384555-28384854 | Rare:89 | ||||
| chr17:28571498-28571698 | Rare:47 | ||||
| chr17:28599004-28599170 | Common:2; Rare:43 | ||||
| chr17:28645046-28645361 | Common:1; Rare:131 |