Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:47163933-47164255 | Common:1; Rare:89 | ||||
chr3:47380812-47381080 | Rare:85 | ||||
chr3:47475812-47476058 | Common:3; Rare:104 | ||||
chr3:48088792-48089065 | Rare:92 | ||||
chr3:48440047-48440307 | Common:1; Rare:98 | ||||
chr3:48898851-48899018 | Rare:51; Clinvar:6 | ||||
chr3:48918787-48918889 | Common:2; Rare:58 | ||||
chr3:49007150-49007424 | Common:2; Rare:111 | ||||
chr3:49029365-49029572 | Common:2; Rare:152 | ||||
chr3:49104738-49104891 | Rare:60; Clinvar (benign):3 | ||||
chr3:49132954-49133148 | Rare:39; Clinvar:2 | ||||
chr3:49340013-49340178 | Common:2; Rare:64 | ||||
chr3:49411909-49412318 | Common:2; Rare:153 | ||||
chr3:49674228-49674398 | Common:1; Rare:64 | ||||
chr3:49689461-49689605 | Rare:45 |