| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42964410-42964546 | Rare:65 | ||||
| chr17:42997996-42998675 | Common:6; Rare:149 | ||||
| chr17:43125281-43125723 | Rare:118; Clinvar:7; Clinvar (benign):6 | ||||
| chr17:43170252-43170559 | Common:3; Rare:66 | ||||
| chr17:43170998-43171267 | Common:1; Rare:91 | ||||
| chr17:43211748-43211901 | Common:2; Rare:34 | ||||
| chr17:43398876-43399002 | Common:1; Rare:39 | ||||
| chr17:43483661-43484046 | Rare:106 | ||||
| chr17:43545851-43546112 | Common:2; Rare:39 | ||||
| chr17:43546232-43546616 | Common:2; Rare:91 | ||||
| chr17:43778900-43779064 | Rare:39 | ||||
| chr17:43833109-43833284 | Common:1; Rare:51 | ||||
| chr17:43900611-43900754 | Rare:43 | ||||
| chr17:44070608-44070947 | Common:3; Rare:118; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44141769-44142042 | Common:1; Rare:70 |