Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:177263426-177263716 | Common:1; Rare:72 | ||||
chr2:177264627-177264832 | Common:2; Rare:64 | ||||
chr2:177392662-177392791 | Rare:33; Clinvar:1 | ||||
chr2:178451120-178451407 | Common:5; Rare:87; Clinvar:3; Clinvar (benign):3 | ||||
chr2:184598160-184598475 | Common:2; Rare:79 | ||||
chr2:186486135-186486330 | Common:3; Rare:61 | ||||
chr2:187554286-187554414 | Rare:26 | ||||
chr2:189783952-189784133 | Common:3; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
chr2:189784378-189784518 | Common:2; Rare:47; Clinvar:4; Clinvar (benign):1 | ||||
chr2:190344004-190344046 | Rare:7 | ||||
chr2:190534688-190534805 | Common:1; Rare:37 | ||||
chr2:197499806-197500133 | Rare:112; Clinvar:1; Clinvar (benign):1 | ||||
chr2:197500269-197500418 | Common:1; Rare:61 | ||||
chr2:200889282-200889474 | Common:2; Rare:73 | ||||
chr2:200963637-200963908 | Common:1; Rare:68 |