| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75289389-75289615 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:75393723-75394072 | Common:1; Rare:81 | ||||
| chr17:75405580-75406080 | Common:2; Rare:133 | ||||
| chr17:75456394-75456732 | Common:2; Rare:108 | ||||
| chr17:75476260-75476770 | Common:3; Rare:92 | ||||
| chr17:75514427-75515425 | Common:4; Rare:216 | ||||
| chr17:75515430-75516030 | Common:4; Rare:152 | ||||
| chr17:75516220-75516590 | Common:6; Rare:91; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:75525483-75525739 | Common:2; Rare:83 | ||||
| chr17:75633830-75634110 | Common:1; Rare:59 | ||||
| chr17:75667111-75667389 | Common:4; Rare:97 | ||||
| chr17:75779728-75780090 | Common:1; Rare:142 | ||||
| chr17:75784535-75784875 | Common:2; Rare:152 | ||||
| chr17:75785747-75786196 | Common:1; Rare:118 | ||||
| chr17:75855204-75855403 | Common:1; Rare:71 |