| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2796200-2796472 | Common:1; Rare:61 | ||||
| chr17:3636233-3636496 | Common:4; Rare:77; Clinvar (benign):1 | ||||
| chr17:3636646-3636779 | Common:1; Rare:31; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:3668552-3668835 | Common:2; Rare:111 | ||||
| chr17:3723767-3723917 | Common:1; Rare:84 | ||||
| chr17:4142592-4142611 | Rare:7 | ||||
| chr17:4142977-4143225 | Rare:87 | ||||
| chr17:4143597-4143735 | Common:4; Rare:79 | ||||
| chr17:4263937-4264089 | Rare:61 | ||||
| chr17:4366634-4366679 | Rare:18 | ||||
| chr17:4704055-4704231 | Rare:95 | ||||
| chr17:4710734-4710815 | Rare:19 | ||||
| chr17:4731280-4731507 | Common:2; Rare:73 | ||||
| chr17:4736328-4736611 | Rare:51 | ||||
| chr17:4738409-4738635 | Common:2; Rare:46 |