| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4704110-4704231 | Rare:69 | ||||
| chr17:4731316-4731498 | Common:2; Rare:60 | ||||
| chr17:4806987-4807223 | Common:4; Rare:71 | ||||
| chr17:4939912-4940344 | Common:2; Rare:128 | ||||
| chr17:4948932-4949165 | Common:1; Rare:82 | ||||
| chr17:4967781-4967843 | Rare:28 | ||||
| chr17:5191838-5192047 | Rare:69 | ||||
| chr17:5419618-5419863 | Common:3; Rare:84 | ||||
| chr17:5420054-5420225 | Rare:68 | ||||
| chr17:5486151-5486602 | Common:5; Rare:154 | ||||
| chr17:5486789-5486925 | Common:4; Rare:44 | ||||
| chr17:5584465-5584617 | Common:1; Rare:31 | ||||
| chr17:6444190-6444472 | Common:2; Rare:88 | ||||
| chr17:6556409-6556722 | Common:2; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:6640651-6641132 | Common:7; Rare:155 |