| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48429327-48429577 | Common:2; Rare:59 | ||||
| chr3:48439971-48440332 | Common:3; Rare:139 | ||||
| chr3:48446555-48446851 | Common:4; Rare:110 | ||||
| chr3:48446950-48447159 | Common:1; Rare:69 | ||||
| chr3:48466015-48466349 | Common:3; Rare:79; Clinvar:6; Clinvar (benign):3 | ||||
| chr3:48472736-48472854 | Common:1; Rare:18 | ||||
| chr3:48472856-48473344 | Common:2; Rare:104 | ||||
| chr3:48479233-48479352 | Rare:43 | ||||
| chr3:48479378-48479625 | Common:2; Rare:27 | ||||
| chr3:48504060-48504337 | Common:2; Rare:85 | ||||
| chr3:48556783-48557417 | Common:3; Rare:160 | ||||
| chr3:48609557-48609834 | Rare:98 | ||||
| chr3:48634844-48635015 | Common:1; Rare:45 | ||||
| chr3:48635347-48635771 | Common:2; Rare:120 | ||||
| chr3:48635828-48635957 | Rare:24 |