| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76557619-76557854 | Common:1; Rare:82 | ||||
| chr17:76563543-76563714 | Rare:31 | ||||
| chr17:76733862-76734136 | Common:3; Rare:55 | ||||
| chr17:77125745-77125806 | Rare:8 | ||||
| chr17:77433894-77434001 | Common:1; Rare:22 | ||||
| chr17:78970979-78971266 | Common:2; Rare:49 | ||||
| chr17:79027638-79027835 | Common:2; Rare:39 | ||||
| chr17:80108320-80108593 | Common:1; Rare:104; Clinvar:9; Clinvar (benign):8; Clinvar (pathogenic):7 | ||||
| chr17:80826880-80827132 | Common:1; Rare:68 | ||||
| chr17:80892830-80893186 | Common:2; Rare:90 | ||||
| chr17:81190640-81191077 | Common:2; Rare:162 | ||||
| chr17:81240527-81240689 | Common:4; Rare:39 | ||||
| chr17:81545770-81546118 | Common:3; Rare:86 | ||||
| chr17:81651702-81651890 | Common:2; Rare:35 | ||||
| chr17:81887552-81887855 | Rare:78 |