| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:74749034-74749221 | Common:1; Rare:59; Clinvar:2 | ||||
| chr17:74776281-74776560 | Common:5; Rare:93 | ||||
| chr17:74893568-74893737 | Common:8; Rare:61 | ||||
| chr17:74972616-74972826 | Common:2; Rare:60 | ||||
| chr17:75012602-75012689 | Rare:21 | ||||
| chr17:75046929-75047196 | Common:1; Rare:81 | ||||
| chr17:75089867-75090133 | Common:4; Rare:49 | ||||
| chr17:75109742-75109988 | Common:3; Rare:64 | ||||
| chr17:75130556-75131084 | Common:3; Rare:185 | ||||
| chr17:75146666-75146744 | Common:1; Rare:19 | ||||
| chr17:75154477-75154618 | Common:1; Rare:65 | ||||
| chr17:75205390-75205730 | Rare:97 | ||||
| chr17:75234402-75234684 | Common:1; Rare:64 | ||||
| chr17:75261559-75261935 | Common:4; Rare:121; Clinvar (benign):2 | ||||
| chr17:75271139-75271379 | Common:2; Rare:45 |