| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128060318-128060655 | Common:2; Rare:67 | ||||
| chr3:130111461-130111753 | Common:3; Rare:72 | ||||
| chr3:131361588-131361946 | Common:3; Rare:111 | ||||
| chr3:131363355-131363684 | Common:5; Rare:51 | ||||
| chr3:132525926-132526185 | Common:1; Rare:56 | ||||
| chr3:132689167-132689439 | Rare:63; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr3:133491013-133491322 | Common:1; Rare:72 | ||||
| chr3:134057735-134058069 | Common:1; Rare:60 | ||||
| chr3:138247884-138248096 | Rare:35 | ||||
| chr3:139452702-139452947 | Rare:39 | ||||
| chr3:139456177-139456422 | Common:3; Rare:44 | ||||
| chr3:139469805-139470168 | Rare:55 | ||||
| chr3:139470551-139470629 | Rare:14 | ||||
| chr3:139471861-139472010 | Rare:21 | ||||
| chr3:139472059-139472326 | Rare:44 |