| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:70169306-70169539 | Common:1; Rare:65 | ||||
| chr17:72120784-72121068 | Rare:76 | ||||
| chr17:73192817-73193067 | Common:15; Rare:99; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:73232100-73232707 | Common:4; Rare:230 | ||||
| chr17:73310906-73311248 | Common:2; Rare:86 | ||||
| chr17:73311956-73312206 | Rare:65 | ||||
| chr17:74213297-74213583 | Common:4; Rare:63 | ||||
| chr17:74748452-74748703 | Common:3; Rare:96 | ||||
| chr17:74776215-74776540 | Common:4; Rare:102 | ||||
| chr17:74873380-74873486 | Common:2; Rare:43 | ||||
| chr17:75012432-75012872 | Common:2; Rare:120 | ||||
| chr17:75042200-75042362 | Rare:38 | ||||
| chr17:75046923-75047293 | Common:2; Rare:119 | ||||
| chr17:75087642-75087983 | Common:3; Rare:74 | ||||
| chr17:75109863-75110014 | Common:1; Rare:44 |