| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:5282055-5282336 | Common:23; Rare:280 | ||||
| chr17:5419562-5419888 | Common:7; Rare:188 | ||||
| chr17:5420088-5420221 | Rare:101 | ||||
| chr17:5468742-5469142 | Common:6; Rare:290 | ||||
| chr17:5486111-5486608 | Common:11; Rare:315 | ||||
| chr17:5486745-5486920 | Common:7; Rare:71 | ||||
| chr17:5584455-5584613 | Common:1; Rare:34 | ||||
| chr17:6444195-6444478 | Common:4; Rare:171 | ||||
| chr17:6556398-6556641 | Common:2; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:6640626-6641199 | Common:15; Rare:315 | ||||
| chr17:6651517-6651806 | Common:2; Rare:174 | ||||
| chr17:7012275-7012759 | Rare:296 | ||||
| chr17:7035773-7036102 | Rare:147 | ||||
| chr17:7219623-7220191 | Common:11; Rare:297; Clinvar:15; Clinvar (benign):15; Clinvar (pathogenic):5 | ||||
| chr17:7234200-7234675 | Common:2; Rare:381 |