| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75220903-75221176 | Common:3; Rare:51 | ||||
| chr17:75221478-75221742 | Common:2; Rare:46 | ||||
| chr17:75235460-75235708 | Common:1; Rare:84; Clinvar (pathogenic):1 | ||||
| chr17:75366195-75366489 | Common:2; Rare:55 | ||||
| chr17:75686552-75686835 | Common:3; Rare:51 | ||||
| chr17:75700242-75700432 | Common:2; Rare:31 | ||||
| chr17:75870390-75870635 | Common:1; Rare:50 | ||||
| chr17:75895286-75895344 | Rare:10 | ||||
| chr17:76057323-76057434 | Rare:20 | ||||
| chr17:76227084-76227117 | Rare:12 | ||||
| chr17:76266455-76266666 | Rare:40 | ||||
| chr17:76372213-76372660 | Common:3; Rare:85 | ||||
| chr17:76423780-76423885 | Common:1; Rare:23 | ||||
| chr17:76500538-76500742 | Common:1; Rare:32 | ||||
| chr17:76557625-76557884 | Common:1; Rare:90 |