| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59619179-59619318 | Rare:35 | ||||
| chr17:59619486-59619914 | Common:3; Rare:147 | ||||
| chr17:59707370-59707765 | Common:4; Rare:105; Clinvar (benign):6 | ||||
| chr17:59837454-59837986 | Common:1; Rare:74 | ||||
| chr17:59892691-59893158 | Rare:121 | ||||
| chr17:59964678-59964867 | Common:2; Rare:83 | ||||
| chr17:60078433-60078748 | Common:1; Rare:79 | ||||
| chr17:60078876-60079095 | Common:6; Rare:82 | ||||
| chr17:60391914-60392591 | Common:4; Rare:198 | ||||
| chr17:60525881-60526023 | Common:2; Rare:47 | ||||
| chr17:60526162-60526311 | Rare:60 | ||||
| chr17:60599577-60599769 | Rare:34 | ||||
| chr17:60599922-60600417 | Common:3; Rare:186 | ||||
| chr17:60677276-60677676 | Common:2; Rare:135 | ||||
| chr17:61863424-61863766 | Common:3; Rare:76; Clinvar:2; Clinvar (benign):2 |