| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:138608917-138609119 | Common:1; Rare:55 | ||||
| chr3:138834718-138835084 | Rare:120 | ||||
| chr3:139343759-139344139 | Rare:110; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:139389568-139389882 | Common:2; Rare:99 | ||||
| chr3:139539554-139539761 | Common:3; Rare:70 | ||||
| chr3:140941593-140941966 | Common:2; Rare:127 | ||||
| chr3:140942095-140942244 | Common:2; Rare:33 | ||||
| chr3:141231679-141231899 | Common:1; Rare:76 | ||||
| chr3:141386753-141387015 | Common:1; Rare:41 | ||||
| chr3:141486857-141487084 | Common:1; Rare:74 | ||||
| chr3:141738131-141738360 | Common:1; Rare:97 | ||||
| chr3:141875596-141875738 | Common:2; Rare:47 | ||||
| chr3:141876009-141876228 | Rare:62 | ||||
| chr3:141876452-141876723 | Common:2; Rare:100 | ||||
| chr3:142149350-142149676 | Common:3; Rare:94 |