| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:19377638-19377793 | Common:2; Rare:42 | ||||
| chr17:19377903-19378039 | Common:1; Rare:32 | ||||
| chr17:19378156-19378577 | Common:2; Rare:100 | ||||
| chr17:19386289-19386718 | Rare:116 | ||||
| chr17:19387436-19387656 | Common:3; Rare:39 | ||||
| chr17:19411148-19411245 | Rare:24 | ||||
| chr17:19648636-19649018 | Common:3; Rare:135; Clinvar (benign):1 | ||||
| chr17:19977820-19977926 | Common:1; Rare:35 | ||||
| chr17:20009188-20009392 | Common:2; Rare:65 | ||||
| chr17:21214090-21214361 | Common:2; Rare:126 | ||||
| chr17:22523306-22523422 | Rare:27 | ||||
| chr17:27293953-27294127 | Common:1; Rare:74 | ||||
| chr17:27294182-27294427 | Common:1; Rare:73 | ||||
| chr17:28042584-28042665 | Rare:12 | ||||
| chr17:28318937-28319232 | Common:3; Rare:101 |