| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:44861811-44861927 | Common:2; Rare:56 | ||||
| chr3:44976113-44976272 | Common:2; Rare:65 | ||||
| chr3:45689180-45689459 | Common:1; Rare:93 | ||||
| chr3:45995725-45995882 | Rare:36; Clinvar:1 | ||||
| chr3:46407048-46407271 | Rare:39 | ||||
| chr3:46693642-46693748 | Common:1; Rare:22 | ||||
| chr3:46863396-46863705 | Common:2; Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:46979525-46979835 | Common:2; Rare:73; Clinvar:1 | ||||
| chr3:46981981-46982003 | Rare:5 | ||||
| chr3:47163915-47164220 | Common:1; Rare:84 | ||||
| chr3:47380790-47381068 | Rare:86 | ||||
| chr3:47475804-47476068 | Common:3; Rare:107 | ||||
| chr3:47513651-47513767 | Rare:39 | ||||
| chr3:47802911-47803212 | Common:1; Rare:87 | ||||
| chr3:48301336-48301449 | Common:1; Rare:34 |