| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108562396-108562699 | Common:9; Rare:126; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:109052359-109052638 | Common:2; Rare:66 | ||||
| chr12:109097867-109098215 | Common:5; Rare:108 | ||||
| chr12:109154557-109154691 | Common:1; Rare:35 | ||||
| chr12:109477287-109477645 | Common:3; Rare:87 | ||||
| chr12:109573488-109573821 | Common:3; Rare:92; Clinvar:3; Clinvar (benign):3 | ||||
| chr12:109880381-109880651 | Common:1; Rare:84 | ||||
| chr12:109900159-109900336 | Rare:62 | ||||
| chr12:109996273-109996439 | Common:2; Rare:49 | ||||
| chr12:110502060-110502331 | Common:1; Rare:96 | ||||
| chr12:110613932-110614203 | Rare:82; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:111685769-111686098 | Rare:124 | ||||
| chr12:111841869-111841986 | Common:2; Rare:39 | ||||
| chr12:112013119-112013468 | Common:1; Rare:124 | ||||
| chr12:113185440-113185748 | Common:7; Rare:113 |