| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59154979-59155453 | Common:2; Rare:133 | ||||
| chr17:59155555-59155787 | Rare:64 | ||||
| chr17:59220394-59220542 | Common:2; Rare:43 | ||||
| chr17:59565446-59565637 | Common:1; Rare:63 | ||||
| chr17:59619562-59620015 | Common:3; Rare:160 | ||||
| chr17:59707388-59707732 | Common:3; Rare:96; Clinvar (benign):4 | ||||
| chr17:59837618-59838023 | Rare:60 | ||||
| chr17:59892709-59893170 | Common:1; Rare:124 | ||||
| chr17:60078877-60078993 | Common:4; Rare:55 | ||||
| chr17:60392019-60392314 | Common:2; Rare:74 | ||||
| chr17:60525939-60526290 | Common:1; Rare:116 | ||||
| chr17:60677689-60677898 | Rare:53 | ||||
| chr17:61863447-61863676 | Common:2; Rare:46; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:62423782-62423909 | Common:1; Rare:44 | ||||
| chr17:63550187-63550513 | Common:2; Rare:74 |