| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:19362691-19362774 | Rare:37 | ||||
| chr17:19378253-19378509 | Common:1; Rare:60 | ||||
| chr17:19648628-19648814 | Common:2; Rare:61 | ||||
| chr17:19977798-19977958 | Common:1; Rare:55 | ||||
| chr17:20155833-20156099 | Common:1; Rare:86 | ||||
| chr17:20868223-20868600 | Common:3; Rare:103 | ||||
| chr17:21043393-21043411 | Rare:8 | ||||
| chr17:21214148-21214340 | Common:2; Rare:86 | ||||
| chr17:27293992-27294132 | Common:1; Rare:60 | ||||
| chr17:28318912-28319269 | Common:3; Rare:128 | ||||
| chr17:28335425-28335810 | Common:1; Rare:87 | ||||
| chr17:28357466-28357655 | Common:5; Rare:93 | ||||
| chr17:28552589-28552841 | Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:28571504-28571813 | Common:1; Rare:76 | ||||
| chr17:28598994-28599170 | Common:2; Rare:49 |