Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:58919480-58919685 | Common:1; Rare:45 | ||||
chr12:58920148-58920375 | Common:2; Rare:71 | ||||
chr12:58920496-58920667 | Common:2; Rare:63 | ||||
chr12:59595789-59596206 | Common:7; Rare:87 | ||||
chr12:62260022-62260493 | Common:1; Rare:173 | ||||
chr12:62260796-62261088 | Rare:72 | ||||
chr12:62466648-62466838 | Rare:66 | ||||
chr12:63779780-63779917 | Common:2; Rare:48 | ||||
chr12:63780099-63780171 | Rare:33 | ||||
chr12:64222233-64222355 | Rare:45 | ||||
chr12:64404227-64404625 | Common:5; Rare:148 | ||||
chr12:64452014-64452340 | Common:1; Rare:114 | ||||
chr12:64752711-64753009 | Common:2; Rare:61; Clinvar (benign):1 | ||||
chr12:64759109-64759501 | Common:1; Rare:124; Clinvar:6; Clinvar (benign):2 | ||||
chr12:64780715-64780787 | Rare:14 |