| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:105236035-105236329 | Common:2; Rare:132 | ||||
| chr12:106084083-106084278 | Common:2; Rare:32 | ||||
| chr12:107685643-107685895 | Common:2; Rare:83 | ||||
| chr12:108562405-108562658 | Common:8; Rare:106; Clinvar:2; Clinvar (benign):3 | ||||
| chr12:109093412-109093629 | Common:2; Rare:79 | ||||
| chr12:109097848-109098244 | Common:5; Rare:126 | ||||
| chr12:109477287-109477643 | Common:3; Rare:87 | ||||
| chr12:109573448-109573832 | Common:3; Rare:121; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109900183-109900360 | Rare:64 | ||||
| chr12:109996217-109996425 | Common:2; Rare:62 | ||||
| chr12:109999087-109999245 | Rare:30 | ||||
| chr12:110468667-110468909 | Rare:60 | ||||
| chr12:110502037-110502314 | Common:1; Rare:97 | ||||
| chr12:111685788-111686085 | Rare:116 | ||||
| chr12:112013119-112013564 | Common:1; Rare:168 |