| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:70169344-70169554 | Common:1; Rare:55 | ||||
| chr17:72120784-72121047 | Rare:70 | ||||
| chr17:73164875-73165132 | Common:2; Rare:75 | ||||
| chr17:73192817-73193081 | Common:15; Rare:108; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:73232137-73232711 | Common:4; Rare:220 | ||||
| chr17:73309908-73310016 | Rare:18 | ||||
| chr17:73311916-73312176 | Rare:71 | ||||
| chr17:74213192-74213583 | Common:4; Rare:78 | ||||
| chr17:74431305-74431408 | Rare:22 | ||||
| chr17:74432016-74432154 | Common:1; Rare:60 | ||||
| chr17:74466389-74466692 | Rare:73 | ||||
| chr17:74748434-74748730 | Common:5; Rare:111 | ||||
| chr17:74776265-74776543 | Common:4; Rare:93 | ||||
| chr17:75012583-75012736 | Common:1; Rare:46 | ||||
| chr17:75046929-75047194 | Common:1; Rare:81 |