| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75997267-75997444 | Rare:34 | ||||
| chr17:76557631-76557841 | Common:1; Rare:74 | ||||
| chr17:77174856-77175043 | Common:2; Rare:39 | ||||
| chr17:77365833-77365981 | Rare:27 | ||||
| chr17:78364703-78364971 | Rare:52 | ||||
| chr17:78379255-78379353 | Rare:17 | ||||
| chr17:80892169-80892373 | Common:4; Rare:44 | ||||
| chr17:81513459-81513518 | Common:2; Rare:20 | ||||
| chr17:81565891-81565997 | Common:1; Rare:22 | ||||
| chr17:81934651-81934892 | Common:2; Rare:66; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:82253199-82253305 | Common:1; Rare:35 | ||||
| chr18:3593921-3594176 | Common:3; Rare:40 | ||||
| chr18:3594992-3595127 | Common:1; Rare:23 | ||||
| chr18:3603441-3603753 | Common:1; Rare:51 | ||||
| chr18:3603996-3604105 | Rare:24 |