| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:106987022-106987307 | Common:5; Rare:79 | ||||
| chr12:107685717-107685950 | Rare:77 | ||||
| chr12:108339253-108339333 | Rare:19 | ||||
| chr12:108515032-108515327 | Common:1; Rare:88 | ||||
| chr12:108561137-108561463 | Common:4; Rare:82 | ||||
| chr12:108562405-108562733 | Common:9; Rare:136; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108731933-108732237 | Common:2; Rare:83 | ||||
| chr12:109052372-109052668 | Common:3; Rare:83 | ||||
| chr12:109098126-109098636 | Common:2; Rare:204; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:109154557-109154799 | Common:2; Rare:59 | ||||
| chr12:109477264-109477664 | Common:3; Rare:107 | ||||
| chr12:109573421-109573845 | Common:5; Rare:142; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr12:109880351-109880675 | Common:1; Rare:97 | ||||
| chr12:109900227-109900364 | Rare:50 | ||||
| chr12:109996294-109996439 | Common:2; Rare:40 |