| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40499747-40499767 | Rare:2 | ||||
| chr17:40820047-40820433 | Rare:84 | ||||
| chr17:41503472-41503758 | Common:2; Rare:84; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:41503817-41504068 | Common:2; Rare:63 | ||||
| chr17:41511178-41511560 | Common:1; Rare:73 | ||||
| chr17:41579621-41579780 | Common:1; Rare:39 | ||||
| chr17:41610073-41610156 | Rare:26 | ||||
| chr17:41610276-41610381 | Common:1; Rare:39 | ||||
| chr17:41610383-41610797 | Common:2; Rare:112; Clinvar (pathogenic):1 | ||||
| chr17:41610852-41611583 | Common:2; Rare:262; Clinvar:2 | ||||
| chr17:41611586-41611613 | Rare:7 | ||||
| chr17:41655664-41656019 | Common:1; Rare:72 | ||||
| chr17:41768838-41769069 | Rare:68; Clinvar:3; Clinvar (benign):4 | ||||
| chr17:41769082-41769454 | Common:2; Rare:117; Clinvar:17; Clinvar (benign):13; Clinvar (pathogenic):1 | ||||
| chr17:41775494-41775630 | Common:1; Rare:26 |