| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42458666-42458921 | Common:1; Rare:96 | ||||
| chr17:42536041-42536275 | Common:3; Rare:72; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:42536548-42536823 | Common:3; Rare:64; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr17:42561968-42562229 | Common:1; Rare:78 | ||||
| chr17:42566886-42567281 | Common:4; Rare:131 | ||||
| chr17:42567368-42567631 | Common:1; Rare:78 | ||||
| chr17:42577616-42578002 | Common:1; Rare:166 | ||||
| chr17:42609308-42609821 | Common:8; Rare:202; Clinvar (benign):2 | ||||
| chr17:42659157-42659430 | Rare:84 | ||||
| chr17:42677167-42677503 | Rare:66 | ||||
| chr17:42681818-42681907 | Rare:22 | ||||
| chr17:42682413-42682792 | Common:3; Rare:82 | ||||
| chr17:42683616-42683819 | Common:2; Rare:35 | ||||
| chr17:42744376-42744524 | Common:1; Rare:35 | ||||
| chr17:42744575-42744808 | Rare:46 |