| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109154557-109154858 | Common:3; Rare:67 | ||||
| chr12:109477260-109477656 | Common:3; Rare:104 | ||||
| chr12:109573421-109573813 | Common:5; Rare:134; Clinvar:6; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr12:109900164-109900336 | Rare:62 | ||||
| chr12:110281015-110281240 | Rare:83 | ||||
| chr12:110445499-110445663 | Rare:42 | ||||
| chr12:110468722-110468915 | Rare:54 | ||||
| chr12:110502051-110502241 | Common:1; Rare:66 | ||||
| chr12:111685752-111686110 | Rare:133 | ||||
| chr12:111766847-111766977 | Rare:40 | ||||
| chr12:111841898-111841981 | Common:1; Rare:25 | ||||
| chr12:112006009-112006145 | Common:3; Rare:16 | ||||
| chr12:112013119-112013468 | Common:1; Rare:124 | ||||
| chr12:113185409-113185777 | Common:10; Rare:139 | ||||
| chr12:113221019-113221319 | Common:2; Rare:86 |