| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75515426-75515955 | Common:4; Rare:132 | ||||
| chr17:75516357-75516597 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:75516873-75517060 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:75525539-75525772 | Common:1; Rare:83 | ||||
| chr17:75588305-75588499 | Common:1; Rare:57 | ||||
| chr17:75667088-75667454 | Common:5; Rare:120 | ||||
| chr17:75764682-75764788 | Common:1; Rare:29 | ||||
| chr17:75764878-75765457 | Common:3; Rare:164; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr17:75779298-75779551 | Common:1; Rare:128 | ||||
| chr17:75779581-75780168 | Common:2; Rare:228 | ||||
| chr17:75784251-75784342 | Rare:22 | ||||
| chr17:75784517-75785242 | Common:9; Rare:274 | ||||
| chr17:75785267-75785409 | Rare:38 | ||||
| chr17:75785737-75785896 | Rare:27 | ||||
| chr17:75855187-75855764 | Common:2; Rare:177 |