| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6851239-6851476 | Rare:57 | ||||
| chr12:6851847-6852141 | Common:1; Rare:78 | ||||
| chr12:6873276-6873495 | Common:2; Rare:61 | ||||
| chr12:6970583-6970969 | Common:4; Rare:118; Clinvar (benign):1 | ||||
| chr12:7108486-7108722 | Common:1; Rare:61 | ||||
| chr12:12357001-12357137 | Common:1; Rare:72 | ||||
| chr12:14567830-14567920 | Rare:17 | ||||
| chr12:14803455-14803715 | Common:1; Rare:68 | ||||
| chr12:21501576-21501839 | Common:1; Rare:62 | ||||
| chr12:21941421-21941497 | Rare:13 | ||||
| chr12:24949003-24949160 | Common:1; Rare:40 | ||||
| chr12:25195122-25195315 | Common:2; Rare:55 | ||||
| chr12:26938271-26938525 | Common:3; Rare:96 | ||||
| chr12:27710694-27710853 | Common:1; Rare:59 | ||||
| chr12:27970188-27970328 | Common:1; Rare:34 |