| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59106699-59106977 | Common:2; Rare:93; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:59155158-59155523 | Common:2; Rare:81 | ||||
| chr17:59155563-59155767 | Rare:56 | ||||
| chr17:59220390-59220607 | Common:3; Rare:62 | ||||
| chr17:59331489-59331779 | Common:2; Rare:95 | ||||
| chr17:59619563-59620020 | Common:3; Rare:160 | ||||
| chr17:59664527-59664906 | Common:4; Rare:61 | ||||
| chr17:59707397-59707742 | Common:3; Rare:93; Clinvar (benign):3 | ||||
| chr17:59837635-59838032 | Rare:59 | ||||
| chr17:59892709-59893280 | Common:1; Rare:158 | ||||
| chr17:59964699-59965102 | Common:2; Rare:122 | ||||
| chr17:60078903-60079035 | Common:5; Rare:59 | ||||
| chr17:60391935-60392221 | Common:2; Rare:84 | ||||
| chr17:60525918-60526311 | Common:2; Rare:132 | ||||
| chr17:62064502-62064803 | Rare:80 |