| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75130775-75131090 | Common:2; Rare:113 | ||||
| chr17:75205375-75205749 | Common:1; Rare:121 | ||||
| chr17:75261590-75261945 | Common:4; Rare:114; Clinvar (benign):2 | ||||
| chr17:75262361-75262539 | Common:4; Rare:78; Clinvar (benign):4 | ||||
| chr17:75271165-75271419 | Common:3; Rare:47 | ||||
| chr17:75393719-75394058 | Common:1; Rare:81 | ||||
| chr17:75456456-75456729 | Rare:84 | ||||
| chr17:75633951-75634099 | Rare:28 | ||||
| chr17:75667136-75667417 | Common:4; Rare:96 | ||||
| chr17:75784558-75784872 | Common:2; Rare:138 | ||||
| chr17:75904871-75905218 | Common:4; Rare:94 | ||||
| chr17:75979069-75979283 | Rare:59; Clinvar:4 | ||||
| chr17:76103676-76103886 | Common:6; Rare:75 | ||||
| chr17:76141243-76141496 | Common:1; Rare:62 | ||||
| chr17:76353621-76353671 | Rare:21 |