| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75205380-75205749 | Common:1; Rare:117 | ||||
| chr17:75261583-75261945 | Common:4; Rare:115; Clinvar (benign):2 | ||||
| chr17:75262350-75262576 | Common:4; Rare:90; Clinvar (benign):4 | ||||
| chr17:75289365-75289731 | Common:3; Rare:116; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:75393815-75394091 | Common:1; Rare:66 | ||||
| chr17:75456465-75456656 | Rare:51 | ||||
| chr17:75515466-75515657 | Common:3; Rare:55 | ||||
| chr17:75667127-75667391 | Common:4; Rare:92 | ||||
| chr17:75721268-75721536 | Common:3; Rare:84; Clinvar:1 | ||||
| chr17:75784564-75784883 | Common:2; Rare:144 | ||||
| chr17:75855293-75855639 | Common:1; Rare:90 | ||||
| chr17:75904849-75905181 | Common:4; Rare:96 | ||||
| chr17:75978601-75978887 | Common:4; Rare:73; Clinvar (pathogenic):1 | ||||
| chr17:75979052-75979283 | Rare:65; Clinvar:4 | ||||
| chr17:76103686-76103876 | Common:5; Rare:66 |