Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:58327235-58327323 | Rare:20 | ||||
chr19:58440134-58440460 | Common:6; Rare:88 | ||||
chr19:58499206-58499538 | Common:2; Rare:105; Clinvar:3 | ||||
chr19:58519754-58520030 | Rare:72 | ||||
chr19:58554939-58555210 | Common:2; Rare:86 | ||||
chr2:264005-264076 | Common:1; Rare:29 | ||||
chr2:264558-264985 | Common:4; Rare:162 | ||||
chr2:677342-677552 | Common:1; Rare:91 | ||||
chr2:1654406-1654655 | Rare:66 | ||||
chr2:1744274-1744626 | Common:2; Rare:118 | ||||
chr2:3377791-3377947 | Rare:42 | ||||
chr2:3379609-3379779 | Common:2; Rare:72 | ||||
chr2:3519485-3519636 | Common:2; Rare:51 | ||||
chr2:3558209-3558715 | Common:6; Rare:187 | ||||
chr2:3575080-3575447 | Common:2; Rare:103; Clinvar:3; Clinvar (benign):6 |