| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59619590-59619935 | Common:3; Rare:122 | ||||
| chr17:59707381-59707751 | Common:4; Rare:103; Clinvar (benign):6 | ||||
| chr17:59837606-59837993 | Rare:55 | ||||
| chr17:59892917-59893140 | Rare:62 | ||||
| chr17:60525914-60526339 | Common:2; Rare:150 | ||||
| chr17:61399522-61399920 | Common:1; Rare:110 | ||||
| chr17:62627485-62627760 | Common:1; Rare:76 | ||||
| chr17:63699818-63700029 | Common:1; Rare:55 | ||||
| chr17:63700032-63700293 | Common:1; Rare:64 | ||||
| chr17:63773527-63773825 | Common:2; Rare:99 | ||||
| chr17:63827050-63827503 | Common:5; Rare:134 | ||||
| chr17:63827918-63828166 | Common:1; Rare:65 | ||||
| chr17:67717672-67717959 | Common:2; Rare:96 | ||||
| chr17:70169301-70169554 | Common:1; Rare:73 | ||||
| chr17:73192819-73193090 | Common:15; Rare:108; Clinvar:2; Clinvar (benign):1 |