| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76737309-76737525 | Common:3; Rare:85 | ||||
| chr17:76737877-76738070 | Common:3; Rare:53 | ||||
| chr17:77450274-77450567 | Common:2; Rare:61 | ||||
| chr17:77451221-77451527 | Common:1; Rare:69 | ||||
| chr17:78187045-78187376 | Common:3; Rare:106 | ||||
| chr17:78840736-78841114 | Common:2; Rare:144 | ||||
| chr17:78979870-78980087 | Common:2; Rare:44 | ||||
| chr17:79009696-79009928 | Common:9; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:79993689-79993791 | Common:1; Rare:21 | ||||
| chr17:80035843-80036012 | Common:1; Rare:61 | ||||
| chr17:80220309-80220469 | Common:1; Rare:62; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415109-80415197 | Common:1; Rare:59 | ||||
| chr17:80415387-80415492 | Common:4; Rare:40 | ||||
| chr17:81239036-81239317 | Common:2; Rare:92 | ||||
| chr17:81666565-81666763 | Common:1; Rare:86 |