Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:47782946-47783214 | Common:2; Rare:119; Clinvar:6; Clinvar (benign):10 | ||||
chr2:48440609-48440839 | Common:7; Rare:106 | ||||
chr2:53767559-53767866 | Common:4; Rare:106 | ||||
chr2:53786851-53787170 | Common:1; Rare:118 | ||||
chr2:53970788-53971126 | Common:10; Rare:113 | ||||
chr2:55050434-55050794 | Common:4; Rare:109 | ||||
chr2:55232306-55232726 | Common:2; Rare:120 | ||||
chr2:58046612-58046836 | Rare:67 | ||||
chr2:58241316-58241431 | Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
chr2:60756112-60756277 | Rare:55 | ||||
chr2:61017171-61017753 | Common:5; Rare:171; Clinvar:2 | ||||
chr2:61144916-61145164 | Common:3; Rare:83 | ||||
chr2:61471167-61471386 | Common:2; Rare:83 | ||||
chr2:61888515-61888727 | Common:1; Rare:89 | ||||
chr2:63588693-63589025 | Rare:104 |