| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28576886-28577082 | Common:2; Rare:56 | ||||
| chr17:28599007-28599121 | Common:1; Rare:29 | ||||
| chr17:28645112-28645314 | Common:1; Rare:71 | ||||
| chr17:28661848-28662281 | Common:1; Rare:158 | ||||
| chr17:28842770-28842885 | Common:1; Rare:37 | ||||
| chr17:28897620-28897747 | Common:1; Rare:41 | ||||
| chr17:29568483-29568740 | Common:4; Rare:83 | ||||
| chr17:30378701-30378946 | Common:1; Rare:79 | ||||
| chr17:30824678-30824872 | Common:3; Rare:71 | ||||
| chr17:30906205-30906315 | Rare:34 | ||||
| chr17:31321610-31321806 | Common:3; Rare:29 | ||||
| chr17:34961389-34961557 | Rare:77 | ||||
| chr17:34980382-34980572 | Common:3; Rare:57 | ||||
| chr17:35242921-35243072 | Rare:48 | ||||
| chr17:35578485-35578682 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):1 |