| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59154955-59155021 | Rare:29 | ||||
| chr17:59155112-59155792 | Common:2; Rare:172 | ||||
| chr17:59619209-59619345 | Common:1; Rare:38 | ||||
| chr17:59619562-59620025 | Common:3; Rare:161 | ||||
| chr17:59707381-59707732 | Common:4; Rare:98; Clinvar (benign):6 | ||||
| chr17:59837609-59838002 | Rare:58 | ||||
| chr17:59892709-59893155 | Rare:118 | ||||
| chr17:59964697-59964817 | Common:2; Rare:52 | ||||
| chr17:60078886-60078984 | Common:4; Rare:49 | ||||
| chr17:60525939-60526307 | Common:1; Rare:123 | ||||
| chr17:61452263-61452429 | Rare:45 | ||||
| chr17:61863439-61863732 | Common:3; Rare:64; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:62423833-62423909 | Rare:26 | ||||
| chr17:63600818-63600922 | Rare:29; Clinvar:2 | ||||
| chr17:63701144-63701228 | Rare:21 |