| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75271161-75271390 | Common:3; Rare:40 | ||||
| chr17:75289373-75289692 | Common:3; Rare:99; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:75667136-75667372 | Common:4; Rare:74 | ||||
| chr17:75784601-75784872 | Common:2; Rare:116 | ||||
| chr17:75855299-75855658 | Common:1; Rare:95 | ||||
| chr17:75941024-75941260 | Common:1; Rare:71 | ||||
| chr17:75979132-75979245 | Rare:31; Clinvar:2 | ||||
| chr17:75979393-75979581 | Rare:54 | ||||
| chr17:76103712-76103867 | Common:4; Rare:49 | ||||
| chr17:76726471-76726874 | Common:5; Rare:148 | ||||
| chr17:76737316-76737525 | Common:3; Rare:81 | ||||
| chr17:76737923-76738062 | Common:1; Rare:37 | ||||
| chr17:77088618-77088767 | Common:1; Rare:39 | ||||
| chr17:77450449-77450720 | Rare:61 | ||||
| chr17:77451265-77451404 | Rare:34 |