| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50763914-50764282 | Common:1; Rare:101 | ||||
| chr12:50924459-50924698 | Common:3; Rare:74 | ||||
| chr12:51048119-51048359 | Common:1; Rare:82 | ||||
| chr12:51173074-51173185 | Rare:20 | ||||
| chr12:51238609-51238789 | Common:8; Rare:61 | ||||
| chr12:51238794-51238910 | Rare:56 | ||||
| chr12:51270275-51270432 | Common:3; Rare:43 | ||||
| chr12:51391608-51391767 | Common:2; Rare:53 | ||||
| chr12:52051152-52051448 | Common:1; Rare:98 | ||||
| chr12:52069848-52070030 | Common:1; Rare:65 | ||||
| chr12:52451399-52451638 | Common:2; Rare:77; Clinvar (pathogenic):1 | ||||
| chr12:52451660-52451854 | Common:3; Rare:66; Clinvar (benign):1 | ||||
| chr12:52473252-52473297 | Rare:20 | ||||
| chr12:52492642-52493404 | Common:5; Rare:239; Clinvar:2; Clinvar (pathogenic):3 | ||||
| chr12:52493457-52493620 | Rare:34 |