| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:74213328-74213578 | Common:4; Rare:54 | ||||
| chr17:74776290-74776540 | Common:4; Rare:80 | ||||
| chr17:75205399-75205730 | Rare:95 | ||||
| chr17:75261590-75261913 | Common:4; Rare:98; Clinvar (benign):1 | ||||
| chr17:75271154-75271424 | Common:3; Rare:50 | ||||
| chr17:75289387-75289606 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:75515474-75515657 | Common:3; Rare:50 | ||||
| chr17:75639935-75640171 | Common:1; Rare:60 | ||||
| chr17:75646100-75646339 | Common:4; Rare:52 | ||||
| chr17:75667127-75667370 | Common:4; Rare:78 | ||||
| chr17:75765137-75765289 | Common:1; Rare:45; Clinvar:1 | ||||
| chr17:75779683-75780095 | Common:1; Rare:167 | ||||
| chr17:75784558-75784872 | Common:2; Rare:138 | ||||
| chr17:75979103-75979283 | Rare:50; Clinvar:4 | ||||
| chr17:75979393-75979488 | Rare:23 |