| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:25195104-25195304 | Common:2; Rare:60 | ||||
| chr12:26937931-26938534 | Common:11; Rare:198 | ||||
| chr12:27022429-27022621 | Common:2; Rare:59 | ||||
| chr12:27523960-27524282 | Rare:79 | ||||
| chr12:27710721-27710879 | Common:2; Rare:66 | ||||
| chr12:28190360-28190506 | Common:1; Rare:47 | ||||
| chr12:30695818-30696166 | Common:3; Rare:83 | ||||
| chr12:30754758-30755167 | Common:4; Rare:152 | ||||
| chr12:31073784-31073892 | Rare:44 | ||||
| chr12:31326106-31326432 | Common:4; Rare:106 | ||||
| chr12:31728995-31729308 | Common:1; Rare:100 | ||||
| chr12:31959269-31959490 | Common:2; Rare:73 | ||||
| chr12:32399850-32399879 | Rare:11 | ||||
| chr12:32679049-32679343 | Common:2; Rare:111; Clinvar (benign):3 | ||||
| chr12:32896760-32896985 | Common:1; Rare:76; Clinvar:4; Clinvar (benign):3 |