| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:104456821-104457223 | Common:1; Rare:133 | ||||
| chr12:104958254-104958459 | Common:4; Rare:60 | ||||
| chr12:104986232-104986364 | Common:2; Rare:52 | ||||
| chr12:105107621-105107818 | Common:1; Rare:92; Clinvar:1 | ||||
| chr12:105195600-105195733 | Rare:34 | ||||
| chr12:105235995-105236300 | Common:3; Rare:124 | ||||
| chr12:106301816-106301912 | Rare:21 | ||||
| chr12:106357451-106357823 | Common:4; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:106774301-106774618 | Common:1; Rare:80 | ||||
| chr12:106955635-106955923 | Rare:104 | ||||
| chr12:107685709-107685934 | Rare:74 | ||||
| chr12:107761036-107761327 | Common:4; Rare:108 | ||||
| chr12:108339056-108339184 | Common:1; Rare:16 | ||||
| chr12:108339185-108339541 | Common:3; Rare:89 | ||||
| chr12:108515005-108515319 | Common:1; Rare:94 |