| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1650056-1650248 | Common:1; Rare:49 | ||||
| chr17:1684780-1685064 | Common:2; Rare:95; Clinvar:7; Clinvar (benign):1 | ||||
| chr17:1716130-1716527 | Common:3; Rare:122 | ||||
| chr17:1717035-1717300 | Common:1; Rare:54 | ||||
| chr17:1762656-1762826 | Common:3; Rare:37 | ||||
| chr17:1783852-1784037 | Common:1; Rare:36 | ||||
| chr17:1829770-1830039 | Common:7; Rare:115 | ||||
| chr17:2029930-2030199 | Common:3; Rare:102; Clinvar (pathogenic):1 | ||||
| chr17:2303305-2303403 | Rare:38 | ||||
| chr17:2303450-2303595 | Rare:54 | ||||
| chr17:2303716-2303987 | Common:2; Rare:103 | ||||
| chr17:2336407-2336518 | Rare:47 | ||||
| chr17:2337363-2337631 | Common:1; Rare:79 | ||||
| chr17:2511757-2511941 | Common:2; Rare:47 | ||||
| chr17:2593478-2593705 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):2 |