| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75878562-75878740 | Common:3; Rare:61 | ||||
| chr17:75904872-75905218 | Common:4; Rare:94 | ||||
| chr17:75940989-75941181 | Rare:65 | ||||
| chr17:75979045-75979283 | Rare:66; Clinvar:4 | ||||
| chr17:75979348-75979495 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr17:76072487-76072603 | Rare:36 | ||||
| chr17:76103688-76103867 | Common:5; Rare:62 | ||||
| chr17:76353585-76353672 | Rare:37 | ||||
| chr17:76353839-76354097 | Rare:89 | ||||
| chr17:76501355-76501516 | Rare:54; Clinvar (benign):3 | ||||
| chr17:76501613-76501763 | Common:1; Rare:23 | ||||
| chr17:76537571-76537826 | Common:1; Rare:70 | ||||
| chr17:76688651-76688880 | Common:4; Rare:49 | ||||
| chr17:76725840-76726133 | Common:1; Rare:79 | ||||
| chr17:76726464-76726898 | Common:5; Rare:167 |