| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:74213319-74213612 | Common:4; Rare:71 | ||||
| chr17:74240787-74240959 | Common:1; Rare:33 | ||||
| chr17:74249176-74249374 | Common:1; Rare:41 | ||||
| chr17:74274178-74274337 | Common:2; Rare:32; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:74748403-74748708 | Common:4; Rare:114 | ||||
| chr17:74776240-74776550 | Common:4; Rare:101 | ||||
| chr17:74872896-74873055 | Common:2; Rare:66; Clinvar (pathogenic):1 | ||||
| chr17:74922851-74922990 | Rare:40; Clinvar:2 | ||||
| chr17:74972700-74972863 | Common:2; Rare:43 | ||||
| chr17:75012554-75012651 | Common:1; Rare:23 | ||||
| chr17:75012655-75012776 | Common:1; Rare:44 | ||||
| chr17:75046923-75047104 | Common:1; Rare:52 | ||||
| chr17:75109853-75109975 | Common:2; Rare:33 | ||||
| chr17:75130797-75131084 | Common:2; Rare:103 | ||||
| chr17:75131492-75131806 | Common:4; Rare:134 |