| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45490713-45490869 | Rare:53 | ||||
| chr17:46033468-46033665 | Common:2; Rare:36 | ||||
| chr17:46192859-46193020 | Common:1; Rare:43 | ||||
| chr17:46193354-46193611 | Common:4; Rare:70 | ||||
| chr17:47189250-47189381 | Rare:37 | ||||
| chr17:47323903-47324034 | Common:1; Rare:44 | ||||
| chr17:47679859-47680055 | Common:1; Rare:45 | ||||
| chr17:47831516-47831819 | Common:1; Rare:76 | ||||
| chr17:47941354-47941732 | Rare:102; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48048069-48048405 | Rare:86 | ||||
| chr17:48107412-48107599 | Common:4; Rare:47 | ||||
| chr17:48908300-48908407 | Common:1; Rare:25 | ||||
| chr17:48944783-48944884 | Common:1; Rare:30 | ||||
| chr17:49210530-49210714 | Rare:30 | ||||
| chr17:49414845-49415145 | Common:2; Rare:76 |