Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:46297173-46297409 | Common:3; Rare:94 | ||||
chr2:46616995-46617166 | Common:5; Rare:59 | ||||
chr2:46915738-46915898 | Common:1; Rare:44; Clinvar:2; Clinvar (benign):1 | ||||
chr2:53786852-53787071 | Rare:71 | ||||
chr2:53970783-53971122 | Common:10; Rare:113 | ||||
chr2:55232256-55232741 | Common:3; Rare:137 | ||||
chr2:55519418-55519780 | Common:1; Rare:107 | ||||
chr2:61017213-61017329 | Common:3; Rare:28 | ||||
chr2:61017429-61017761 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):2 | ||||
chr2:61144935-61145128 | Common:2; Rare:58 | ||||
chr2:61471164-61471342 | Common:1; Rare:65 | ||||
chr2:61888420-61888729 | Common:1; Rare:142 | ||||
chr2:63840824-63841126 | Common:1; Rare:85 | ||||
chr2:65056203-65056421 | Rare:72 | ||||
chr2:65227597-65227882 | Rare:81 |