Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:53786852-53787184 | Common:1; Rare:125 | ||||
chr2:53970774-53971157 | Common:11; Rare:141 | ||||
chr2:54456081-54456517 | Common:1; Rare:161 | ||||
chr2:54456969-54457285 | Common:2; Rare:124 | ||||
chr2:55050215-55050245 | Rare:9 | ||||
chr2:55050263-55050416 | Common:1; Rare:61 | ||||
chr2:55050441-55050754 | Common:4; Rare:95 | ||||
chr2:55519409-55519760 | Common:1; Rare:101 | ||||
chr2:55543808-55544060 | Common:4; Rare:66 | ||||
chr2:55923709-55923887 | Common:4; Rare:59; Clinvar (benign):8 | ||||
chr2:58046598-58046717 | Rare:38 | ||||
chr2:58046755-58046845 | Rare:33 | ||||
chr2:58047224-58047284 | Rare:19 | ||||
chr2:58241316-58241381 | Rare:44; Clinvar:3; Clinvar (benign):1 | ||||
chr2:60881307-60881664 | Common:2; Rare:135 |