| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75261590-75261935 | Common:4; Rare:108; Clinvar (benign):2 | ||||
| chr17:75271165-75271296 | Common:1; Rare:28 | ||||
| chr17:75393724-75394011 | Common:1; Rare:72 | ||||
| chr17:75515419-75515644 | Common:3; Rare:64 | ||||
| chr17:75667144-75667396 | Common:4; Rare:86 | ||||
| chr17:75779657-75779914 | Common:1; Rare:132 | ||||
| chr17:75784595-75784872 | Common:2; Rare:117 | ||||
| chr17:75855269-75855636 | Common:1; Rare:101 | ||||
| chr17:75941030-75941182 | Rare:47 | ||||
| chr17:75979067-75979283 | Rare:60; Clinvar:4 | ||||
| chr17:75979358-75979465 | Common:1; Rare:32; Clinvar (benign):1 | ||||
| chr17:76103703-76103876 | Common:4; Rare:61 | ||||
| chr17:76501377-76501575 | Rare:66; Clinvar (benign):3 | ||||
| chr17:76725983-76726076 | Common:1; Rare:19 | ||||
| chr17:76726462-76726893 | Common:5; Rare:166 |