Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:28870267-28870418 | Rare:56 | ||||
chr2:31414698-31414933 | Common:2; Rare:43; Clinvar (benign):1 | ||||
chr2:32039761-32039870 | Rare:32 | ||||
chr2:32165745-32165886 | Common:1; Rare:45 | ||||
chr2:33599242-33599593 | Common:1; Rare:123 | ||||
chr2:37084319-37084563 | Common:3; Rare:94 | ||||
chr2:37196434-37196512 | Rare:24 | ||||
chr2:37231563-37231696 | Common:4; Rare:72; Clinvar (benign):3 | ||||
chr2:38076149-38076309 | Common:1; Rare:40 | ||||
chr2:38875906-38876010 | Common:1; Rare:26 | ||||
chr2:39437283-39437447 | Common:2; Rare:56 | ||||
chr2:46617019-46617246 | Common:6; Rare:89 | ||||
chr2:46915724-46915908 | Common:1; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
chr2:48440707-48440815 | Common:5; Rare:51 | ||||
chr2:53767559-53767866 | Common:4; Rare:106 |