| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:156826187-156826374 | Common:1; Rare:63 | ||||
| chr3:157160084-157160295 | Rare:88 | ||||
| chr3:158105726-158105902 | Common:5; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:158571049-158571238 | Rare:62 | ||||
| chr3:158710972-158711191 | Common:2; Rare:32 | ||||
| chr3:158732159-158732353 | Common:6; Rare:55 | ||||
| chr3:158732447-158732623 | Common:1; Rare:65 | ||||
| chr3:158801984-158802168 | Common:2; Rare:86 | ||||
| chr3:160399196-160399290 | Rare:22; Clinvar:1 | ||||
| chr3:160565278-160565845 | Common:3; Rare:191 | ||||
| chr3:161105075-161105384 | Common:4; Rare:87 | ||||
| chr3:167734835-167735071 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735559-167735752 | Rare:48 | ||||
| chr3:169773331-169773418 | Rare:25 | ||||
| chr3:169966654-169966851 | Common:1; Rare:77 |