| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75721187-75721595 | Common:3; Rare:127; Clinvar:2 | ||||
| chr17:75756452-75756853 | Rare:162; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:75779274-75779538 | Common:1; Rare:134 | ||||
| chr17:75779651-75780047 | Common:1; Rare:163 | ||||
| chr17:75784563-75784886 | Common:2; Rare:145 | ||||
| chr17:75844688-75844960 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:75855272-75855650 | Common:1; Rare:107 | ||||
| chr17:75878562-75878702 | Common:3; Rare:52 | ||||
| chr17:75904871-75905027 | Common:2; Rare:52 | ||||
| chr17:75979003-75979339 | Rare:94; Clinvar:4 | ||||
| chr17:75979386-75979490 | Common:1; Rare:28; Clinvar (benign):1 | ||||
| chr17:76011580-76011819 | Common:1; Rare:69 | ||||
| chr17:76027100-76027473 | Common:1; Rare:97 | ||||
| chr17:76072496-76072595 | Rare:30 | ||||
| chr17:76103693-76103867 | Common:5; Rare:60 |