| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59154955-59155051 | Rare:35 | ||||
| chr17:59155115-59155517 | Common:2; Rare:93 | ||||
| chr17:59220405-59220607 | Common:3; Rare:60 | ||||
| chr17:59331407-59331822 | Common:3; Rare:134 | ||||
| chr17:59565462-59565746 | Common:1; Rare:105 | ||||
| chr17:59619518-59619629 | Common:1; Rare:33 | ||||
| chr17:59619794-59620057 | Common:1; Rare:96 | ||||
| chr17:59683605-59683984 | Rare:62 | ||||
| chr17:59707397-59707732 | Common:3; Rare:91; Clinvar (benign):3 | ||||
| chr17:59837667-59837970 | Rare:43 | ||||
| chr17:59892739-59893260 | Common:1; Rare:148 | ||||
| chr17:59964669-59965050 | Common:2; Rare:122 | ||||
| chr17:59965051-59965181 | Rare:27 | ||||
| chr17:60078876-60078974 | Common:4; Rare:49 | ||||
| chr17:60256651-60256716 | Rare:10 |