| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123201838-123201967 | Common:1; Rare:41 | ||||
| chr3:123585489-123585553 | Rare:11 | ||||
| chr3:123700954-123701337 | Rare:75; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:125375231-125375391 | Rare:43 | ||||
| chr3:125520162-125520307 | Rare:42 | ||||
| chr3:127598229-127598446 | Common:3; Rare:57 | ||||
| chr3:127822446-127822475 | Rare:5 | ||||
| chr3:127822491-127822757 | Rare:59 | ||||
| chr3:128052202-128052500 | Common:2; Rare:99 | ||||
| chr3:128879434-128879675 | Common:4; Rare:120; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129161339-129161460 | Common:1; Rare:37 | ||||
| chr3:129183822-129184081 | Common:2; Rare:89 | ||||
| chr3:129249534-129249680 | Common:1; Rare:46 | ||||
| chr3:129278761-129278882 | Common:4; Rare:40 | ||||
| chr3:129316283-129316377 | Common:1; Rare:29 |