| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46348080-46348457 | Common:2; Rare:76 | ||||
| chr2:46349479-46349694 | Rare:48 | ||||
| chr2:46350270-46350600 | Common:1; Rare:64 | ||||
| chr2:46351518-46351623 | Common:1; Rare:16 | ||||
| chr2:46351853-46352069 | Rare:56 | ||||
| chr2:46358594-46358938 | Common:2; Rare:80 | ||||
| chr2:46360664-46360916 | Rare:76; Clinvar (benign):3 | ||||
| chr2:46365026-46365248 | Common:1; Rare:46 | ||||
| chr2:46366800-46366930 | Common:1; Rare:30 | ||||
| chr2:46371798-46371831 | Rare:3 | ||||
| chr2:46373412-46373679 | Common:3; Rare:49 | ||||
| chr2:46579534-46579623 | Rare:12 | ||||
| chr2:46587447-46587499 | Common:1; Rare:10 | ||||
| chr2:46589830-46589924 | Rare:21 | ||||
| chr2:46591051-46591147 | Rare:18 |