| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:60392765-60392964 | Rare:33 | ||||
| chr17:60525659-60525828 | Common:1; Rare:56 | ||||
| chr17:60525852-60526043 | Common:2; Rare:65 | ||||
| chr17:60526072-60526358 | Rare:106 | ||||
| chr17:60599944-60600417 | Common:3; Rare:182 | ||||
| chr17:60600431-60600531 | Common:1; Rare:20 | ||||
| chr17:60600630-60600742 | Rare:34 | ||||
| chr17:60677275-60677524 | Common:1; Rare:55 | ||||
| chr17:60677633-60677960 | Common:1; Rare:91 | ||||
| chr17:60678116-60678130 | Rare:1 | ||||
| chr17:60887456-60887796 | Common:1; Rare:73 | ||||
| chr17:61399201-61399412 | Rare:47 | ||||
| chr17:61399510-61400084 | Common:1; Rare:168 | ||||
| chr17:61400214-61400477 | Rare:97; Clinvar (pathogenic):1 | ||||
| chr17:61400609-61400669 | Rare:19 |