| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:124863685-124864028 | Common:4; Rare:89 | ||||
| chr12:124989053-124989297 | Common:5; Rare:68 | ||||
| chr12:125065303-125065470 | Common:2; Rare:65 | ||||
| chr12:128823972-128824089 | Rare:35 | ||||
| chr12:128853393-128853614 | Common:2; Rare:61 | ||||
| chr12:130871735-130872126 | Common:4; Rare:162 | ||||
| chr12:131929081-131929296 | Common:9; Rare:61; Clinvar:1 | ||||
| chr12:132687274-132687701 | Common:4; Rare:157; Clinvar:12; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132829065-132829217 | Rare:76 | ||||
| chr12:132887552-132887859 | Rare:91 | ||||
| chr12:132956252-132956426 | Common:1; Rare:38 | ||||
| chr12:132986247-132986452 | Rare:51 | ||||
| chr12:133080183-133080459 | Common:7; Rare:86 | ||||
| chr12:133130238-133130652 | Common:7; Rare:137 | ||||
| chr13:19633416-19633747 | Common:1; Rare:122 |