| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59106636-59107001 | Common:3; Rare:115; Clinvar:6; Clinvar (benign):4 | ||||
| chr17:59155150-59155544 | Common:2; Rare:91 | ||||
| chr17:59331421-59331789 | Common:3; Rare:120 | ||||
| chr17:59619557-59620108 | Common:3; Rare:189 | ||||
| chr17:59655697-59656022 | Rare:51 | ||||
| chr17:59707392-59707732 | Common:3; Rare:94; Clinvar (benign):4 | ||||
| chr17:59837618-59838066 | Common:1; Rare:68 | ||||
| chr17:59892884-59893161 | Common:1; Rare:83 | ||||
| chr17:59964706-59965092 | Common:2; Rare:118 | ||||
| chr17:60078903-60079005 | Common:4; Rare:46 | ||||
| chr17:60525934-60526297 | Common:2; Rare:120 | ||||
| chr17:60600082-60600220 | Common:2; Rare:37 | ||||
| chr17:61399568-61399887 | Rare:90 | ||||
| chr17:61400333-61400486 | Rare:60 | ||||
| chr17:63446253-63446515 | Rare:88 |