| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50221350-50221559 | Rare:47 | ||||
| chr12:50766777-50766983 | Common:2; Rare:36 | ||||
| chr12:50933800-50933996 | Common:1; Rare:26 | ||||
| chr12:51395586-51395668 | Common:2; Rare:20 | ||||
| chr12:51405845-51406160 | Common:1; Rare:55 | ||||
| chr12:51408016-51408256 | Common:3; Rare:45 | ||||
| chr12:51846968-51847072 | Rare:23 | ||||
| chr12:51863832-51863994 | Rare:31 | ||||
| chr12:51864961-51865194 | Common:2; Rare:54 | ||||
| chr12:51872459-51872564 | Rare:23 | ||||
| chr12:51913385-51913486 | Rare:23; Clinvar (benign):1 | ||||
| chr12:53664976-53665284 | Common:1; Rare:43 | ||||
| chr12:54081869-54081957 | Rare:13 | ||||
| chr12:54359067-54359525 | Common:3; Rare:114 | ||||
| chr12:56190239-56190335 | Common:1; Rare:47 |