| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75289372-75289606 | Common:2; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:75393717-75394034 | Common:1; Rare:78 | ||||
| chr17:75456456-75456729 | Rare:84 | ||||
| chr17:75515409-75515703 | Common:3; Rare:88 | ||||
| chr17:75516354-75516563 | Rare:62; Clinvar (pathogenic):1 | ||||
| chr17:75525483-75525804 | Common:3; Rare:103 | ||||
| chr17:75558228-75558627 | Common:3; Rare:105 | ||||
| chr17:75563086-75563431 | Common:6; Rare:109 | ||||
| chr17:75568627-75568801 | Rare:71 | ||||
| chr17:75587970-75588523 | Common:4; Rare:155 | ||||
| chr17:75624133-75624445 | Common:2; Rare:130 | ||||
| chr17:75630653-75630966 | Common:14; Rare:131; Clinvar (benign):1 | ||||
| chr17:75633519-75633782 | Rare:52 | ||||
| chr17:75633845-75633938 | Rare:21 | ||||
| chr17:75633959-75634126 | Common:1; Rare:35 |