Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:53786851-53787169 | Common:1; Rare:117 | ||||
chr2:53970786-53971126 | Common:10; Rare:113 | ||||
chr2:54115510-54115642 | Rare:39 | ||||
chr2:55050309-55050386 | Rare:29 | ||||
chr2:55050441-55050818 | Common:4; Rare:115 | ||||
chr2:55232249-55232719 | Common:3; Rare:129 | ||||
chr2:55618849-55619031 | Common:1; Rare:45 | ||||
chr2:58046591-58046717 | Rare:39 | ||||
chr2:58046759-58046845 | Rare:31 | ||||
chr2:60881327-60881624 | Common:2; Rare:122 | ||||
chr2:61017429-61017750 | Common:1; Rare:94; Clinvar:2 | ||||
chr2:61144921-61145165 | Common:3; Rare:82 | ||||
chr2:61536503-61536767 | Common:2; Rare:76 | ||||
chr2:61854019-61854212 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
chr2:61888575-61888700 | Common:1; Rare:52 |