| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76726436-76726893 | Common:5; Rare:172 | ||||
| chr17:76737318-76737691 | Common:4; Rare:130 | ||||
| chr17:76737894-76738153 | Common:4; Rare:73 | ||||
| chr17:77320078-77320317 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:78168527-78168662 | Common:1; Rare:42 | ||||
| chr17:78187045-78187391 | Common:3; Rare:114 | ||||
| chr17:78782219-78782555 | Common:9; Rare:106 | ||||
| chr17:78840736-78841114 | Common:2; Rare:144 | ||||
| chr17:80035852-80036149 | Common:2; Rare:95 | ||||
| chr17:80220309-80220453 | Rare:57; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415109-80415195 | Common:1; Rare:57 | ||||
| chr17:81239036-81239327 | Common:2; Rare:95 | ||||
| chr17:81666540-81666763 | Common:1; Rare:99 | ||||
| chr17:81683685-81684057 | Common:4; Rare:188 | ||||
| chr17:81703294-81703517 | Common:2; Rare:62; Clinvar (benign):2 |