| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75456435-75456745 | Common:1; Rare:95 | ||||
| chr17:75492153-75492457 | Rare:59 | ||||
| chr17:75515462-75515640 | Common:3; Rare:51 | ||||
| chr17:75516375-75516603 | Common:2; Rare:65; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:75629401-75629541 | Rare:40 | ||||
| chr17:75667100-75667417 | Common:4; Rare:111 | ||||
| chr17:75668447-75668552 | Rare:44 | ||||
| chr17:75779444-75779480 | Rare:20 | ||||
| chr17:75784894-75784922 | Rare:12 | ||||
| chr17:75904857-75905218 | Common:5; Rare:102 | ||||
| chr17:75979100-75979287 | Rare:52; Clinvar:4 | ||||
| chr17:75979398-75979495 | Rare:24 | ||||
| chr17:76072305-76072443 | Common:4; Rare:64 | ||||
| chr17:76103647-76103867 | Common:5; Rare:76 | ||||
| chr17:76265557-76265899 | Common:2; Rare:94 |