| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:45689180-45689468 | Common:1; Rare:97 | ||||
| chr3:45995729-45995868 | Rare:31; Clinvar:1 | ||||
| chr3:46208282-46208586 | Common:3; Rare:44 | ||||
| chr3:46407023-46407275 | Rare:47 | ||||
| chr3:46693649-46693774 | Common:1; Rare:34 | ||||
| chr3:46979511-46979852 | Common:2; Rare:86; Clinvar:1 | ||||
| chr3:47163933-47164220 | Common:1; Rare:77 | ||||
| chr3:47380799-47381141 | Rare:114 | ||||
| chr3:47381436-47381609 | Rare:41 | ||||
| chr3:47475816-47476068 | Common:3; Rare:105 | ||||
| chr3:47513345-47513530 | Common:1; Rare:57 | ||||
| chr3:47513672-47513788 | Rare:34 | ||||
| chr3:47803014-47803192 | Common:1; Rare:57 | ||||
| chr3:48301340-48301495 | Common:1; Rare:44 | ||||
| chr3:48440066-48440401 | Common:1; Rare:144 |