| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:74748417-74748712 | Common:6; Rare:185 | ||||
| chr17:74776232-74776560 | Common:9; Rare:186 | ||||
| chr17:74873240-74873540 | Common:9; Rare:187 | ||||
| chr17:75012565-75012736 | Common:2; Rare:78 | ||||
| chr17:75020100-75020750 | Common:5; Rare:154 | ||||
| chr17:75046883-75047256 | Common:4; Rare:230 | ||||
| chr17:75087573-75088043 | Common:10; Rare:191 | ||||
| chr17:75109853-75110034 | Common:4; Rare:93 | ||||
| chr17:75130620-75131200 | Common:7; Rare:388 | ||||
| chr17:75131492-75131877 | Common:8; Rare:252 | ||||
| chr17:75154390-75154890 | Common:2; Rare:271 | ||||
| chr17:75182506-75182670 | Common:3; Rare:84 | ||||
| chr17:75182840-75183191 | Common:4; Rare:216 | ||||
| chr17:75205301-75205759 | Common:2; Rare:287 | ||||
| chr17:75261559-75261967 | Common:8; Rare:279; Clinvar (benign):8 |