| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59892913-59893140 | Rare:63 | ||||
| chr17:60525935-60526288 | Common:2; Rare:118 | ||||
| chr17:61399590-61399897 | Rare:81 | ||||
| chr17:62627145-62627457 | Common:2; Rare:81 | ||||
| chr17:62627509-62627764 | Common:1; Rare:72 | ||||
| chr17:62628028-62628144 | Rare:19 | ||||
| chr17:63773521-63773858 | Common:2; Rare:111 | ||||
| chr17:63827057-63827504 | Common:5; Rare:130 | ||||
| chr17:67717740-67717972 | Rare:80 | ||||
| chr17:68247908-68248117 | Common:5; Rare:89 | ||||
| chr17:70169372-70169541 | Common:1; Rare:45 | ||||
| chr17:73232137-73232458 | Common:1; Rare:148 | ||||
| chr17:74776240-74776520 | Common:4; Rare:89 | ||||
| chr17:75046943-75047201 | Common:1; Rare:76 | ||||
| chr17:75261587-75261981 | Common:4; Rare:136; Clinvar (benign):4 |