| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:69060908-69061125 | Common:1; Rare:34 | ||||
| chr17:69141733-69142111 | Common:2; Rare:70 | ||||
| chr17:69327066-69327346 | Common:2; Rare:91 | ||||
| chr17:70169327-70169554 | Common:1; Rare:61 | ||||
| chr17:73232243-73232707 | Common:3; Rare:164 | ||||
| chr17:74213326-74213578 | Common:4; Rare:54 | ||||
| chr17:74466219-74466439 | Common:2; Rare:46 | ||||
| chr17:74466578-74466693 | Rare:36 | ||||
| chr17:74776281-74776540 | Common:4; Rare:87 | ||||
| chr17:75012521-75012719 | Common:2; Rare:55 | ||||
| chr17:75046929-75047194 | Common:1; Rare:81 | ||||
| chr17:75109881-75109969 | Common:1; Rare:22 | ||||
| chr17:75182836-75183182 | Common:2; Rare:122 | ||||
| chr17:75205370-75205730 | Common:1; Rare:108 | ||||
| chr17:75261570-75261935 | Common:4; Rare:116; Clinvar (benign):2 |