| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59106707-59106970 | Common:2; Rare:86; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:59155112-59155784 | Common:2; Rare:171 | ||||
| chr17:59209772-59210052 | Common:1; Rare:67 | ||||
| chr17:59619538-59620103 | Common:3; Rare:197 | ||||
| chr17:59707378-59707732 | Common:4; Rare:99; Clinvar (benign):6 | ||||
| chr17:59837635-59837988 | Rare:52 | ||||
| chr17:59892714-59893140 | Rare:113 | ||||
| chr17:60078886-60078971 | Common:4; Rare:44 | ||||
| chr17:60392004-60392355 | Common:2; Rare:90 | ||||
| chr17:60525939-60526398 | Common:1; Rare:156 | ||||
| chr17:60677686-60677902 | Common:1; Rare:54 | ||||
| chr17:62423781-62423897 | Common:1; Rare:42 | ||||
| chr17:63700116-63700348 | Common:1; Rare:60 | ||||
| chr17:63701144-63701207 | Rare:16 | ||||
| chr17:63774066-63774262 | Common:9; Rare:99 |