| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:68291249-68291513 | Common:1; Rare:76 | ||||
| chr17:68511796-68512039 | Rare:60 | ||||
| chr17:68512284-68512506 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:69327122-69327334 | Common:1; Rare:69 | ||||
| chr17:69414576-69414750 | Rare:38 | ||||
| chr17:69502259-69502412 | Rare:28 | ||||
| chr17:72120784-72121034 | Rare:67 | ||||
| chr17:73164869-73165077 | Common:2; Rare:65 | ||||
| chr17:73232242-73232707 | Common:3; Rare:165 | ||||
| chr17:74748407-74748641 | Common:2; Rare:81 | ||||
| chr17:74776329-74776499 | Common:4; Rare:48 | ||||
| chr17:75012586-75012689 | Rare:23 | ||||
| chr17:75109880-75109981 | Common:1; Rare:25 | ||||
| chr17:75205427-75205730 | Rare:86 | ||||
| chr17:75261590-75261935 | Common:4; Rare:108; Clinvar (benign):2 |