| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42773369-42773527 | Rare:45 | ||||
| chr17:42798685-42798959 | Rare:75 | ||||
| chr17:42833015-42833149 | Common:2; Rare:28 | ||||
| chr17:42833275-42833672 | Common:2; Rare:126 | ||||
| chr17:42833813-42834116 | Common:2; Rare:73 | ||||
| chr17:42964408-42964546 | Rare:65 | ||||
| chr17:42998346-42998762 | Common:4; Rare:107 | ||||
| chr17:43024634-43024762 | Common:1; Rare:28 | ||||
| chr17:43025084-43025514 | Rare:110 | ||||
| chr17:43125305-43125662 | Rare:95; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:43169859-43170039 | Common:3; Rare:28 | ||||
| chr17:43170405-43170637 | Common:3; Rare:42 | ||||
| chr17:43170952-43171294 | Common:1; Rare:123 | ||||
| chr17:43398878-43399071 | Common:2; Rare:70 | ||||
| chr17:43483778-43484070 | Rare:87 |