| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109097425-109097686 | Rare:91; Clinvar:3 | ||||
| chr12:109097841-109098242 | Common:5; Rare:127 | ||||
| chr12:109477279-109477650 | Common:3; Rare:92 | ||||
| chr12:109573421-109573863 | Common:5; Rare:148; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr12:109900202-109900360 | Rare:62 | ||||
| chr12:109996232-109996445 | Common:2; Rare:64 | ||||
| chr12:109999085-109999167 | Rare:13 | ||||
| chr12:110073262-110073295 | Common:1; Rare:9 | ||||
| chr12:110073477-110073749 | Rare:50 | ||||
| chr12:110124125-110124502 | Common:2; Rare:112 | ||||
| chr12:110124728-110124800 | Rare:13 | ||||
| chr12:110124803-110124872 | Rare:7 | ||||
| chr12:110171790-110172071 | Common:1; Rare:40 | ||||
| chr12:110172294-110172341 | Rare:14 | ||||
| chr12:110281003-110281193 | Common:1; Rare:74 |