| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41689301-41689621 | Common:2; Rare:113 | ||||
| chr17:41812593-41813198 | Common:3; Rare:151; Clinvar:8 | ||||
| chr17:41818191-41818448 | Common:1; Rare:93; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:41865377-41865559 | Rare:72 | ||||
| chr17:42017133-42017486 | Rare:114 | ||||
| chr17:42017577-42017642 | Rare:24 | ||||
| chr17:42017644-42017689 | Rare:8 | ||||
| chr17:42154946-42155283 | Common:4; Rare:87 | ||||
| chr17:42423123-42423398 | Common:1; Rare:72; Clinvar:2 | ||||
| chr17:42458730-42458963 | Common:3; Rare:86 | ||||
| chr17:42566888-42567149 | Common:3; Rare:91 | ||||
| chr17:42577642-42577802 | Rare:77 | ||||
| chr17:42609328-42609752 | Common:8; Rare:178; Clinvar (benign):2 | ||||
| chr17:42761027-42761254 | Rare:65 | ||||
| chr17:42773362-42773501 | Rare:43 |