| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:126083986-126084212 | Common:2; Rare:73 | ||||
| chr3:126476066-126476339 | Common:5; Rare:39 | ||||
| chr3:127590725-127590913 | Common:2; Rare:39 | ||||
| chr3:127598220-127598458 | Common:3; Rare:70 | ||||
| chr3:127672805-127673011 | Common:3; Rare:99 | ||||
| chr3:128052208-128052475 | Common:2; Rare:90 | ||||
| chr3:128153373-128153499 | Rare:36 | ||||
| chr3:128487889-128488219 | Common:1; Rare:82 | ||||
| chr3:128488550-128488657 | Common:1; Rare:24 | ||||
| chr3:128488995-128489263 | Rare:58 | ||||
| chr3:128879401-128879669 | Common:4; Rare:129; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129001220-129001308 | Common:1; Rare:19 | ||||
| chr3:129001511-129001621 | Common:1; Rare:31 | ||||
| chr3:129060663-129060810 | Rare:36 | ||||
| chr3:129183332-129183442 | Rare:32 |