Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:15242765-15242967 | Rare:33 | ||||
chr3:15738217-15738513 | Common:3; Rare:59 | ||||
chr3:39177696-39177790 | Common:6; Rare:10 | ||||
chr3:39411668-39411956 | Rare:78; Clinvar (pathogenic):1 | ||||
chr3:40453175-40453417 | Common:4; Rare:53 | ||||
chr3:41237744-41238048 | Common:1; Rare:75 | ||||
chr3:51393024-51393132 | Rare:38 | ||||
chr3:52502335-52502671 | Common:2; Rare:65 | ||||
chr3:57903416-57903642 | Rare:37 | ||||
chr3:64560725-64561024 | Common:2; Rare:52 | ||||
chr3:64561120-64561553 | Common:4; Rare:87 | ||||
chr3:64561759-64561827 | Common:2; Rare:28 | ||||
chr3:64572441-64572530 | Common:3; Rare:16 | ||||
chr3:64685046-64685171 | Rare:31 | ||||
chr3:72100917-72101042 | Rare:28 |