| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:39443300-39443446 | Rare:48; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:39619760-39619919 | Common:1; Rare:26 | ||||
| chr12:40692075-40692579 | Common:1; Rare:132 | ||||
| chr12:40827686-40828004 | Rare:53 | ||||
| chr12:41437510-41437757 | Rare:53 | ||||
| chr12:42325964-42326205 | Common:1; Rare:75 | ||||
| chr12:42484295-42484359 | Common:1; Rare:15 | ||||
| chr12:43758745-43758996 | Common:2; Rare:69; Clinvar:2 | ||||
| chr12:43806229-43806385 | Common:2; Rare:54 | ||||
| chr12:44876054-44876394 | Common:3; Rare:107 | ||||
| chr12:45215987-45216226 | Common:1; Rare:72 | ||||
| chr12:45729421-45729742 | Common:1; Rare:89 | ||||
| chr12:45990504-45990919 | Common:2; Rare:133 | ||||
| chr12:46372690-46373056 | Common:1; Rare:143 | ||||
| chr12:47705962-47706088 | Rare:57 |