Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:38071309-38071586 | Common:1; Rare:51 | ||||
chr2:39245060-39245107 | Rare:9 | ||||
chr2:39438094-39438226 | Rare:24 | ||||
chr2:39512197-39512414 | Common:2; Rare:37 | ||||
chr2:41914262-41914370 | Common:3; Rare:24 | ||||
chr2:41915022-41915225 | Common:5; Rare:35 | ||||
chr2:41933909-41934008 | Rare:20 | ||||
chr2:41934077-41934257 | Rare:37 | ||||
chr2:42810448-42810598 | Common:1; Rare:87 | ||||
chr2:42827703-42827876 | Common:3; Rare:52 | ||||
chr2:43219907-43220146 | Common:1; Rare:52 | ||||
chr2:43324330-43324587 | Rare:43 | ||||
chr2:46299583-46299929 | Common:2; Rare:84 | ||||
chr2:46306408-46306411 | |||||
chr2:46376353-46376753 | Common:5; Rare:130; Clinvar:2; Clinvar (benign):6 |