| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28597655-28597809 | Rare:20 | ||||
| chr17:28644088-28644167 | Rare:28 | ||||
| chr17:28722125-28722138 | Common:1; Rare:1 | ||||
| chr17:28738010-28738310 | Common:1; Rare:95; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:28738719-28739032 | Rare:77; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:28741441-28741717 | Rare:87; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:28743159-28743341 | Rare:28 | ||||
| chr17:28745238-28745507 | Common:2; Rare:71 | ||||
| chr17:28763216-28763415 | Rare:30 | ||||
| chr17:28871325-28871484 | Rare:23 | ||||
| chr17:28892182-28892465 | Rare:48 | ||||
| chr17:28893028-28893140 | Rare:19 | ||||
| chr17:28893615-28893945 | Rare:68 | ||||
| chr17:29138655-29138837 | Rare:35 | ||||
| chr17:29139017-29139251 | Common:2; Rare:39 |