| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42964410-42964597 | Common:1; Rare:75 | ||||
| chr17:42980373-42980576 | Common:1; Rare:58 | ||||
| chr17:42980722-42980938 | Common:1; Rare:53 | ||||
| chr17:42998202-42998537 | Common:4; Rare:89 | ||||
| chr17:43022296-43022494 | Rare:59 | ||||
| chr17:43025078-43025378 | Rare:75 | ||||
| chr17:43125359-43125723 | Rare:80; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:43170185-43170718 | Common:3; Rare:112 | ||||
| chr17:43170966-43171273 | Common:1; Rare:104 | ||||
| chr17:43398869-43398996 | Common:1; Rare:37 | ||||
| chr17:43778872-43779048 | Rare:41 | ||||
| chr17:43833114-43833322 | Common:2; Rare:60 | ||||
| chr17:43900566-43900766 | Rare:71 | ||||
| chr17:43907468-43907608 | Common:1; Rare:49 | ||||
| chr17:44070612-44070947 | Common:3; Rare:116; Clinvar:4; Clinvar (benign):2 |