| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75619067-75619402 | Rare:100 | ||||
| chr17:75619457-75619733 | Common:4; Rare:67 | ||||
| chr17:75620047-75620767 | Common:5; Rare:203 | ||||
| chr17:75621121-75621569 | Common:8; Rare:140 | ||||
| chr17:75623848-75624013 | Common:7; Rare:62 | ||||
| chr17:75624181-75624450 | Common:1; Rare:116 | ||||
| chr17:75624645-75624914 | Common:1; Rare:91 | ||||
| chr17:75625033-75625191 | Rare:65 | ||||
| chr17:75625198-75625660 | Common:2; Rare:131 | ||||
| chr17:75633459-75633787 | Rare:82 | ||||
| chr17:75646131-75646412 | Common:5; Rare:64 | ||||
| chr17:75667136-75667466 | Common:5; Rare:111 | ||||
| chr17:75721179-75721601 | Common:3; Rare:131; Clinvar:3 | ||||
| chr17:75756698-75757104 | Common:4; Rare:181; Clinvar:10; Clinvar (benign):2 | ||||
| chr17:75784595-75784872 | Common:2; Rare:117 |