| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59331441-59331753 | Common:2; Rare:106 | ||||
| chr17:59565419-59565711 | Common:1; Rare:111 | ||||
| chr17:59566106-59566219 | Rare:25 | ||||
| chr17:59619149-59619257 | Rare:31 | ||||
| chr17:59619263-59619430 | Common:4; Rare:43 | ||||
| chr17:59619440-59620012 | Common:4; Rare:192 | ||||
| chr17:59706409-59706751 | Common:3; Rare:70 | ||||
| chr17:59707352-59707796 | Common:4; Rare:111; Clinvar (benign):6 | ||||
| chr17:59707944-59707998 | Common:1; Rare:6 | ||||
| chr17:59837288-59838202 | Common:5; Rare:139 | ||||
| chr17:59892650-59892752 | Rare:21 | ||||
| chr17:59892913-59893192 | Common:1; Rare:86 | ||||
| chr17:59893546-59893587 | Rare:8 | ||||
| chr17:59893607-59893874 | Rare:41 | ||||
| chr17:59964014-59964310 | Rare:55 |