Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:176002221-176002416 | Common:3; Rare:86 | ||||
chr2:176116670-176116799 | Rare:26 | ||||
chr2:176129555-176129753 | Rare:105 | ||||
chr2:176130505-176130813 | Common:2; Rare:165 | ||||
chr2:176188503-176188678 | Common:1; Rare:67 | ||||
chr2:176188911-176189081 | Common:2; Rare:61 | ||||
chr2:176269414-176269505 | Common:1; Rare:45 | ||||
chr2:177212402-177212821 | Common:5; Rare:171 | ||||
chr2:177263402-177263651 | Common:1; Rare:56 | ||||
chr2:177264533-177264930 | Common:2; Rare:112 | ||||
chr2:177392672-177393070 | Common:2; Rare:139; Clinvar:6; Clinvar (benign):4 | ||||
chr2:177552761-177553064 | Common:4; Rare:93 | ||||
chr2:178450727-178450897 | Rare:57 | ||||
chr2:178451090-178451382 | Common:6; Rare:85; Clinvar:4; Clinvar (benign):3 | ||||
chr2:178478424-178478680 | Common:1; Rare:82 |