| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:45689180-45689464 | Common:1; Rare:96 | ||||
| chr3:45995749-45995875 | Rare:27; Clinvar:1 | ||||
| chr3:45995879-45995981 | Common:3; Rare:18 | ||||
| chr3:46407057-46407268 | Rare:39 | ||||
| chr3:46565659-46565832 | Common:1; Rare:35 | ||||
| chr3:46566198-46566464 | Rare:54 | ||||
| chr3:46693642-46693801 | Common:1; Rare:38 | ||||
| chr3:46863244-46863770 | Common:4; Rare:125; Clinvar:8; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr3:46882154-46882415 | Common:1; Rare:79 | ||||
| chr3:46979555-46979838 | Common:1; Rare:61; Clinvar:1 | ||||
| chr3:47163915-47164239 | Common:1; Rare:90 | ||||
| chr3:47380780-47381090 | Rare:104 | ||||
| chr3:47381432-47381538 | Rare:25 | ||||
| chr3:47475812-47476084 | Common:3; Rare:109 | ||||
| chr3:47513312-47513466 | Common:1; Rare:33 |