| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108562361-108562661 | Common:13; Rare:222; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:108731449-108731686 | Common:2; Rare:88 | ||||
| chr12:108731870-108732300 | Common:6; Rare:201 | ||||
| chr12:108857550-108857769 | Rare:212 | ||||
| chr12:109052469-109052654 | Common:6; Rare:105 | ||||
| chr12:109097091-109097726 | Rare:242; Clinvar:5 | ||||
| chr12:109097961-109098221 | Common:9; Rare:161 | ||||
| chr12:109154474-109154828 | Common:4; Rare:121 | ||||
| chr12:109309685-109310000 | Common:1; Rare:186 | ||||
| chr12:109477277-109477679 | Common:6; Rare:200 | ||||
| chr12:109573026-109573426 | Common:7; Rare:125; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:109573453-109573869 | Common:6; Rare:253; Clinvar:12; Clinvar (benign):12; Clinvar (pathogenic):4 | ||||
| chr12:109880375-109880696 | Common:3; Rare:160 | ||||
| chr12:109900077-109900337 | Rare:133 | ||||
| chr12:109900370-109900830 | Common:1; Rare:119 |