| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15651822-15651998 | Rare:24 | ||||
| chr17:15684216-15684479 | Common:3; Rare:74 | ||||
| chr17:15699441-15699826 | Common:5; Rare:109 | ||||
| chr17:15944837-15944866 | Rare:6 | ||||
| chr17:15944934-15945138 | Common:1; Rare:47 | ||||
| chr17:15945216-15945321 | Common:2; Rare:26 | ||||
| chr17:15999285-15999907 | Common:5; Rare:287; Clinvar:8; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr17:16000314-16000349 | Rare:17 | ||||
| chr17:16215067-16215123 | Rare:17 | ||||
| chr17:16215434-16215741 | Common:3; Rare:135 | ||||
| chr17:16216990-16217025 | Rare:8 | ||||
| chr17:16217030-16217365 | Rare:100; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr17:16352873-16353261 | Common:1; Rare:118 | ||||
| chr17:16353358-16353653 | Common:1; Rare:105 | ||||
| chr17:16380538-16381401 | Common:8; Rare:290 |