| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75393763-75394056 | Common:1; Rare:65 | ||||
| chr17:75405621-75405832 | Common:1; Rare:76 | ||||
| chr17:75639946-75640161 | Common:1; Rare:51 | ||||
| chr17:75667136-75667409 | Common:4; Rare:95 | ||||
| chr17:75756451-75756859 | Rare:164; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:75784563-75784868 | Common:2; Rare:133 | ||||
| chr17:75904871-75905218 | Common:4; Rare:94 | ||||
| chr17:75979077-75979283 | Rare:56; Clinvar:4 | ||||
| chr17:75979393-75979490 | Rare:25 | ||||
| chr17:76027295-76027529 | Rare:51 | ||||
| chr17:76103712-76103867 | Common:4; Rare:49 | ||||
| chr17:76725773-76726060 | Rare:80 | ||||
| chr17:76726491-76726893 | Common:5; Rare:149 | ||||
| chr17:76737318-76737678 | Common:4; Rare:126 | ||||
| chr17:77287789-77287958 | Rare:20 |