| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76737317-76737570 | Common:3; Rare:98 | ||||
| chr17:76737886-76738119 | Common:4; Rare:67 | ||||
| chr17:76872572-76872899 | Common:1; Rare:99 | ||||
| chr17:77088606-77088767 | Common:1; Rare:44 | ||||
| chr17:77140660-77141038 | Common:2; Rare:134 | ||||
| chr17:77287759-77287995 | Rare:32 | ||||
| chr17:77319888-77319961 | Common:1; Rare:21; Clinvar (benign):1 | ||||
| chr17:77320074-77320317 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:77323129-77323270 | Rare:34 | ||||
| chr17:77404977-77405088 | Rare:30 | ||||
| chr17:78168516-78168638 | Rare:39 | ||||
| chr17:78187029-78187376 | Common:3; Rare:114 | ||||
| chr17:78378409-78378687 | Common:2; Rare:87 | ||||
| chr17:78782261-78782554 | Common:9; Rare:93 | ||||
| chr17:78840756-78841105 | Common:2; Rare:134 |