Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:37059610-37059727 | Common:1; Rare:40 | ||||
chr13:39038047-39038407 | Common:1; Rare:90 | ||||
chr13:40771167-40771400 | Common:3; Rare:65 | ||||
chr13:41060912-41061617 | Common:18; Rare:269 | ||||
chr13:43786928-43786992 | Rare:21 | ||||
chr13:44989456-44989621 | Rare:58 | ||||
chr13:45341040-45341417 | Common:4; Rare:179 | ||||
chr13:46052713-46052847 | Common:2; Rare:34 | ||||
chr13:48037648-48037742 | Rare:41 | ||||
chr13:48303671-48303882 | Rare:70; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr13:49247838-49248087 | Rare:75 | ||||
chr13:49444002-49444281 | Common:1; Rare:96 | ||||
chr13:50081971-50082264 | Common:1; Rare:81 | ||||
chr13:52450576-52450788 | Rare:63 | ||||
chr13:52455301-52455550 | Common:3; Rare:88 |