| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:106357372-106357829 | Common:4; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:106357939-106358138 | Common:3; Rare:92 | ||||
| chr12:106774078-106774376 | Common:3; Rare:78 | ||||
| chr12:106774560-106774714 | Common:1; Rare:50 | ||||
| chr12:106955430-106955841 | Common:3; Rare:150 | ||||
| chr12:106956657-106956853 | Rare:33 | ||||
| chr12:106987040-106987349 | Common:5; Rare:87 | ||||
| chr12:107093514-107093642 | Rare:49 | ||||
| chr12:107685620-107685965 | Common:2; Rare:109 | ||||
| chr12:107761065-107761279 | Common:3; Rare:82 | ||||
| chr12:108515038-108515313 | Common:1; Rare:83 | ||||
| chr12:108561136-108561443 | Common:3; Rare:76 | ||||
| chr12:108562361-108562673 | Common:8; Rare:125; Clinvar:2; Clinvar (benign):4 | ||||
| chr12:108598034-108598270 | Rare:55 | ||||
| chr12:108730413-108730445 | Rare:7 |