| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:68346625-68346843 | Common:1; Rare:47 | ||||
| chr17:68511760-68512081 | Rare:87 | ||||
| chr17:69115928-69116067 | Common:1; Rare:22 | ||||
| chr17:69117964-69118045 | Rare:22 | ||||
| chr17:69327118-69327372 | Common:1; Rare:80 | ||||
| chr17:69414617-69414744 | Rare:23 | ||||
| chr17:73192817-73193065 | Common:15; Rare:98; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:73232120-73232709 | Common:4; Rare:227 | ||||
| chr17:74442860-74443062 | Common:4; Rare:46 | ||||
| chr17:74466610-74466693 | Rare:28 | ||||
| chr17:74736710-74736931 | Common:1; Rare:52 | ||||
| chr17:74748387-74748644 | Common:2; Rare:88 | ||||
| chr17:74776275-74776477 | Common:4; Rare:64 | ||||
| chr17:74873347-74873493 | Common:4; Rare:57 | ||||
| chr17:75012592-75012719 | Common:1; Rare:37 |