| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59685296-59685802 | Common:2; Rare:94 | ||||
| chr17:59706986-59707272 | Common:3; Rare:61 | ||||
| chr17:59707378-59707742 | Common:4; Rare:101; Clinvar (benign):6 | ||||
| chr17:59729476-59729760 | Common:2; Rare:45 | ||||
| chr17:59837635-59838054 | Rare:63 | ||||
| chr17:59838302-59838779 | Rare:90 | ||||
| chr17:59892712-59893313 | Common:1; Rare:167 | ||||
| chr17:59964697-59965096 | Common:2; Rare:123 | ||||
| chr17:60078894-60078986 | Common:4; Rare:46 | ||||
| chr17:60391920-60392273 | Common:2; Rare:100 | ||||
| chr17:60525792-60526294 | Common:2; Rare:165 | ||||
| chr17:60600007-60600229 | Common:3; Rare:79 | ||||
| chr17:60677651-60677902 | Common:1; Rare:68 | ||||
| chr17:61863459-61863706 | Common:1; Rare:51; Clinvar:2 | ||||
| chr17:62477941-62478056 | Common:1; Rare:36 |