| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:68944788-68944878 | Rare:29 | ||||
| chr17:68955240-68955470 | Rare:41 | ||||
| chr17:69327029-69327364 | Common:2; Rare:106 | ||||
| chr17:69414607-69414743 | Rare:25 | ||||
| chr17:70169344-70169539 | Common:1; Rare:52 | ||||
| chr17:72120787-72121068 | Rare:75 | ||||
| chr17:72121453-72121638 | Rare:54 | ||||
| chr17:73164848-73165028 | Common:2; Rare:53 | ||||
| chr17:73192550-73192631 | Common:1; Rare:30 | ||||
| chr17:73192817-73193090 | Common:15; Rare:113; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:73227647-73227806 | Common:2; Rare:33 | ||||
| chr17:73231902-73232722 | Common:9; Rare:280 | ||||
| chr17:73233589-73233822 | Common:3; Rare:55 | ||||
| chr17:73644478-73644547 | Common:1; Rare:21 | ||||
| chr17:74203604-74204011 | Common:4; Rare:162 |