| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40318069-40318305 | Common:1; Rare:49 | ||||
| chr17:40342038-40342195 | Common:1; Rare:30 | ||||
| chr17:40501567-40501740 | Rare:38 | ||||
| chr17:40937263-40937394 | Common:1; Rare:16 | ||||
| chr17:41525322-41525496 | Common:1; Rare:37 | ||||
| chr17:41528264-41528499 | Common:1; Rare:55; Clinvar:1 | ||||
| chr17:41583334-41583583 | Rare:78; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr17:41586529-41586667 | Common:4; Rare:56; Clinvar:1; Clinvar (benign):5 | ||||
| chr17:41586866-41587192 | Common:3; Rare:72 | ||||
| chr17:41624741-41624922 | Rare:46 | ||||
| chr17:41688627-41688897 | Common:1; Rare:88 | ||||
| chr17:41786039-41786152 | Rare:24 | ||||
| chr17:41812900-41813029 | Rare:38 | ||||
| chr17:41835998-41836333 | Common:3; Rare:90 | ||||
| chr17:41966610-41966860 | Common:1; Rare:87 |