| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59106692-59106977 | Common:2; Rare:96; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:59155124-59155763 | Common:2; Rare:162 | ||||
| chr17:59331428-59331822 | Common:3; Rare:127 | ||||
| chr17:59619557-59620172 | Common:3; Rare:207 | ||||
| chr17:59664656-59664857 | Rare:35 | ||||
| chr17:59683678-59683985 | Rare:50 | ||||
| chr17:59685352-59685802 | Common:2; Rare:87 | ||||
| chr17:59707388-59707742 | Common:3; Rare:98; Clinvar (benign):4 | ||||
| chr17:59837667-59838084 | Common:1; Rare:63 | ||||
| chr17:59838227-59838967 | Common:1; Rare:148 | ||||
| chr17:59892714-59893311 | Common:1; Rare:167 | ||||
| chr17:59964699-59965092 | Common:2; Rare:121 | ||||
| chr17:60078910-60078974 | Common:4; Rare:35 | ||||
| chr17:60391920-60392316 | Common:2; Rare:111 | ||||
| chr17:60392352-60392501 | Common:2; Rare:48 |