| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44899378-44899729 | Common:2; Rare:110; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:45051406-45051676 | Common:1; Rare:88 | ||||
| chr17:45060939-45061358 | Common:3; Rare:114 | ||||
| chr17:45148165-45148477 | Common:1; Rare:92 | ||||
| chr17:45161498-45161814 | Common:1; Rare:81 | ||||
| chr17:45221631-45221737 | Rare:29 | ||||
| chr17:45222257-45222453 | Rare:48 | ||||
| chr17:46192586-46192732 | Common:2; Rare:26; Clinvar (benign):2 | ||||
| chr17:46192834-46193005 | Common:1; Rare:42 | ||||
| chr17:46193467-46193601 | Common:1; Rare:39 | ||||
| chr17:47189172-47189568 | Common:1; Rare:108 | ||||
| chr17:47323791-47324044 | Common:3; Rare:97 | ||||
| chr17:47649420-47650013 | Common:2; Rare:205 | ||||
| chr17:47831458-47831662 | Rare:65 | ||||
| chr17:48047764-48047902 | Common:1; Rare:30 |