Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:46617019-46617275 | Common:7; Rare:112 | ||||
chr2:46915721-46915908 | Common:1; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
chr2:46916033-46916135 | Common:2; Rare:29 | ||||
chr2:47905496-47905848 | Common:3; Rare:174 | ||||
chr2:48440619-48440816 | Common:6; Rare:81 | ||||
chr2:53767559-53767886 | Common:5; Rare:116 | ||||
chr2:53786883-53787148 | Rare:95 | ||||
chr2:53970666-53971163 | Common:13; Rare:194 | ||||
chr2:55050309-55050397 | Rare:33 | ||||
chr2:55050441-55050784 | Common:4; Rare:103 | ||||
chr2:55112598-55112706 | Rare:26 | ||||
chr2:55232249-55232726 | Common:3; Rare:134 | ||||
chr2:55419851-55420186 | Common:5; Rare:134 | ||||
chr2:58046603-58046875 | Common:2; Rare:84 | ||||
chr2:58047220-58047284 | Rare:21 |