| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123700942-123701321 | Rare:79; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:124730387-124730474 | Common:2; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:125375237-125375395 | Rare:44 | ||||
| chr3:125520153-125520315 | Rare:50 | ||||
| chr3:126084107-126084219 | Common:1; Rare:48 | ||||
| chr3:126180496-126180647 | Rare:28 | ||||
| chr3:126180854-126181008 | Common:1; Rare:47 | ||||
| chr3:127628949-127629227 | Common:1; Rare:94 | ||||
| chr3:128052202-128052526 | Common:2; Rare:110 | ||||
| chr3:128123767-128124038 | Rare:70 | ||||
| chr3:128153365-128153499 | Rare:38 | ||||
| chr3:128488554-128488651 | Common:1; Rare:20 | ||||
| chr3:128493201-128493295 | Rare:34 | ||||
| chr3:128726067-128726200 | Common:1; Rare:33; Clinvar:2 | ||||
| chr3:128879421-128879675 | Common:4; Rare:124; Clinvar:2; Clinvar (benign):2 |