| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75721159-75721567 | Common:3; Rare:126; Clinvar:2 | ||||
| chr17:75756467-75756788 | Rare:133; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:75756792-75757100 | Common:4; Rare:144; Clinvar:9; Clinvar (benign):1 | ||||
| chr17:75784563-75784872 | Common:2; Rare:136 | ||||
| chr17:75830487-75830626 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:75844695-75844957 | Common:1; Rare:56; Clinvar:1 | ||||
| chr17:75855286-75855693 | Common:1; Rare:110 | ||||
| chr17:75904871-75904995 | Common:1; Rare:45 | ||||
| chr17:75978993-75979283 | Rare:84; Clinvar:4 | ||||
| chr17:75979352-75979490 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr17:76027291-76027531 | Rare:53 | ||||
| chr17:76072487-76072658 | Rare:53 | ||||
| chr17:76103703-76103882 | Common:5; Rare:61 | ||||
| chr17:76264904-76265207 | Common:1; Rare:70 | ||||
| chr17:76353612-76353677 | Rare:27 |