| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75979394-75979495 | Rare:24 | ||||
| chr17:76084068-76084287 | Rare:51 | ||||
| chr17:76537685-76537841 | Common:1; Rare:32 | ||||
| chr17:76537922-76537984 | Rare:23 | ||||
| chr17:76726405-76726874 | Common:5; Rare:171 | ||||
| chr17:76737328-76737524 | Common:2; Rare:72 | ||||
| chr17:76737877-76738135 | Common:4; Rare:74 | ||||
| chr17:77319211-77319553 | Common:4; Rare:84; Clinvar (benign):2 | ||||
| chr17:77376152-77376309 | Common:2; Rare:34 | ||||
| chr17:77426434-77426567 | Common:1; Rare:26 | ||||
| chr17:78187004-78187372 | Common:3; Rare:127 | ||||
| chr17:78360069-78360170 | Common:1; Rare:24 | ||||
| chr17:78840758-78841004 | Common:2; Rare:91 | ||||
| chr17:79839369-79839653 | Rare:87 | ||||
| chr17:80147141-80147337 | Common:4; Rare:65 |