| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:44761594-44761804 | Common:3; Rare:76 | ||||
| chr3:44861789-44861925 | Common:2; Rare:63 | ||||
| chr3:44976113-44976278 | Common:2; Rare:67 | ||||
| chr3:45388454-45388616 | Rare:41 | ||||
| chr3:45689177-45689464 | Common:1; Rare:97 | ||||
| chr3:45995814-45995848 | Rare:11; Clinvar:1 | ||||
| chr3:46979533-46979806 | Common:1; Rare:60; Clinvar:1 | ||||
| chr3:47163887-47164220 | Common:1; Rare:93; Clinvar (pathogenic):1 | ||||
| chr3:47380780-47381068 | Rare:89 | ||||
| chr3:47475812-47476058 | Common:3; Rare:104 | ||||
| chr3:47513658-47513788 | Rare:40 | ||||
| chr3:47578247-47578363 | Rare:30 | ||||
| chr3:47802859-47803199 | Common:1; Rare:107 | ||||
| chr3:47890976-47891177 | Rare:46 | ||||
| chr3:47891179-47891491 | Rare:70 |