| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:45689002-45689064 | Rare:56 | ||||
| chr3:45689073-45689494 | Common:3; Rare:155 | ||||
| chr3:45689548-45689660 | Common:1; Rare:28 | ||||
| chr3:45842049-45842329 | Common:1; Rare:77 | ||||
| chr3:45915702-45916077 | Common:1; Rare:85 | ||||
| chr3:45995511-45995988 | Common:3; Rare:88; Clinvar:1 | ||||
| chr3:46208297-46208569 | Common:3; Rare:42 | ||||
| chr3:46407448-46407532 | Common:1; Rare:16 | ||||
| chr3:46976352-46976534 | Common:2; Rare:70 | ||||
| chr3:46976674-46977082 | Common:4; Rare:99 | ||||
| chr3:46979448-46979909 | Common:3; Rare:115; Clinvar:2 | ||||
| chr3:47162886-47163239 | Common:1; Rare:67 | ||||
| chr3:47163656-47163685 | Rare:11 | ||||
| chr3:47163843-47164411 | Common:1; Rare:147; Clinvar (pathogenic):1 | ||||
| chr3:47164419-47164621 | Rare:47 |