| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42804269-42804664 | Common:2; Rare:108 | ||||
| chr3:43621835-43622342 | Common:2; Rare:146; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690817-43690993 | Common:3; Rare:95; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:44477655-44477694 | Rare:7 | ||||
| chr3:44624913-44625063 | Common:2; Rare:41 | ||||
| chr3:44761577-44761774 | Common:3; Rare:78 | ||||
| chr3:44861760-44861927 | Common:2; Rare:76 | ||||
| chr3:44976095-44976295 | Common:3; Rare:84 | ||||
| chr3:45388378-45388604 | Common:1; Rare:58 | ||||
| chr3:45689075-45689468 | Common:3; Rare:146 | ||||
| chr3:45995776-45995848 | Rare:18; Clinvar:1 | ||||
| chr3:46882162-46882462 | Common:1; Rare:89 | ||||
| chr3:46979525-46979803 | Common:2; Rare:65; Clinvar:1 | ||||
| chr3:47163933-47164269 | Common:1; Rare:94 | ||||
| chr3:47380838-47381068 | Rare:62 |