| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53299410-53299710 | Common:2; Rare:78 | ||||
| chr12:53299830-53300126 | Rare:109 | ||||
| chr12:53300331-53300468 | Common:2; Rare:26 | ||||
| chr12:53321117-53321136 | Rare:1 | ||||
| chr12:53321145-53321214 | Common:1; Rare:11 | ||||
| chr12:53321226-53321437 | Common:1; Rare:77; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr12:53451811-53452111 | Rare:72 | ||||
| chr12:53452268-53452373 | Rare:20 | ||||
| chr12:53452590-53452870 | Common:2; Rare:96 | ||||
| chr12:53453252-53453463 | Common:1; Rare:44 | ||||
| chr12:53453920-53454293 | Rare:80 | ||||
| chr12:53455461-53455527 | Rare:14 | ||||
| chr12:53467798-53468313 | Common:1; Rare:118 | ||||
| chr12:53468618-53468833 | Rare:49 | ||||
| chr12:53486140-53486456 | Common:1; Rare:61 |