Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:3575120-3575345 | Common:2; Rare:65; Clinvar:2; Clinvar (benign):5 | ||||
chr2:9423443-9423676 | Rare:73 | ||||
chr2:17753759-17753874 | Common:1; Rare:45 | ||||
chr2:26244602-26244965 | Common:2; Rare:131; Clinvar:5; Clinvar (benign):7 | ||||
chr2:27211781-27212065 | Common:3; Rare:100 | ||||
chr2:27212271-27212360 | Common:1; Rare:45 | ||||
chr2:27356754-27356770 | Rare:4 | ||||
chr2:27370310-27370641 | Common:1; Rare:131 | ||||
chr2:27583025-27583095 | Rare:25 | ||||
chr2:27628983-27629052 | Common:1; Rare:34 | ||||
chr2:28870275-28870418 | Rare:50 | ||||
chr2:32039782-32039851 | Rare:23 | ||||
chr2:37084328-37084520 | Common:3; Rare:66 | ||||
chr2:37231568-37231684 | Common:3; Rare:58; Clinvar (benign):3 | ||||
chr2:38875902-38876043 | Common:1; Rare:46 |