| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:21166075-21166197 | Rare:25 | ||||
| chr17:21214123-21214361 | Common:2; Rare:110 | ||||
| chr17:21214565-21214597 | Rare:14 | ||||
| chr17:21253251-21253567 | Common:5; Rare:99 | ||||
| chr17:21287843-21288183 | Rare:93 | ||||
| chr17:27293981-27294173 | Common:2; Rare:80 | ||||
| chr17:27294310-27294398 | Common:1; Rare:28 | ||||
| chr17:28335366-28335841 | Common:1; Rare:113 | ||||
| chr17:28357355-28357699 | Common:10; Rare:161; Clinvar (pathogenic):1 | ||||
| chr17:28370239-28370348 | Rare:14 | ||||
| chr17:28571497-28571654 | Rare:38 | ||||
| chr17:28576857-28577061 | Common:2; Rare:53 | ||||
| chr17:28599003-28599177 | Common:2; Rare:45 | ||||
| chr17:28645084-28645310 | Common:1; Rare:85 | ||||
| chr17:28661877-28661935 | Rare:30 |