| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121440844-121441133 | Common:3; Rare:73 | ||||
| chr12:121580222-121580360 | Rare:42 | ||||
| chr12:121580997-121581033 | Rare:4 | ||||
| chr12:121802905-121803109 | Common:1; Rare:54 | ||||
| chr12:121803121-121803311 | Rare:54 | ||||
| chr12:121858860-121858934 | Common:1; Rare:13; Clinvar (benign):2 | ||||
| chr12:121888637-121888876 | Common:2; Rare:79 | ||||
| chr12:122225747-122225912 | Rare:54 | ||||
| chr12:122266389-122266582 | Common:2; Rare:75 | ||||
| chr12:122526849-122527291 | Common:4; Rare:162 | ||||
| chr12:122871985-122872040 | Rare:13 | ||||
| chr12:122896048-122896182 | Rare:72 | ||||
| chr12:122975083-122975248 | Common:1; Rare:44 | ||||
| chr12:122980421-122980938 | Common:2; Rare:156 | ||||
| chr12:123105457-123105649 | Common:1; Rare:36 |