| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75289387-75289668 | Common:2; Rare:87; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:75393754-75394023 | Common:1; Rare:61 | ||||
| chr17:75515426-75515729 | Common:3; Rare:91 | ||||
| chr17:75557660-75557773 | Rare:25 | ||||
| chr17:75633622-75634115 | Common:1; Rare:95 | ||||
| chr17:75646128-75646354 | Common:4; Rare:52 | ||||
| chr17:75667136-75667406 | Common:4; Rare:94 | ||||
| chr17:75784584-75784881 | Common:2; Rare:135 | ||||
| chr17:75855287-75855699 | Common:1; Rare:113 | ||||
| chr17:75979008-75979283 | Rare:79; Clinvar:4 | ||||
| chr17:75979385-75979490 | Common:1; Rare:28; Clinvar (benign):1 | ||||
| chr17:76072465-76072636 | Rare:59 | ||||
| chr17:76103668-76103867 | Common:5; Rare:72 | ||||
| chr17:76353579-76353676 | Rare:40 | ||||
| chr17:76725787-76726085 | Common:1; Rare:83 |