Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:48998438-48998518 | Common:1; Rare:17 | ||||
chr3:49802472-49802707 | Common:1; Rare:38 | ||||
chr3:51959377-51959649 | Common:1; Rare:59 | ||||
chr3:52311609-52311811 | Common:2; Rare:38 | ||||
chr3:52407257-52407432 | Rare:47; Clinvar:3; Clinvar (benign):7 | ||||
chr3:53197135-53197294 | Common:1; Rare:43 | ||||
chr3:53927233-53927399 | Common:1; Rare:53 | ||||
chr3:54025787-54025996 | Common:1; Rare:37 | ||||
chr3:55584849-55585064 | Common:1; Rare:47 | ||||
chr3:57952270-57952602 | Rare:49 | ||||
chr3:59606705-59606870 | Common:2; Rare:29 | ||||
chr3:64685839-64686077 | Common:1; Rare:59 | ||||
chr3:65177311-65177440 | Rare:29 | ||||
chr3:69451652-69451938 | Common:2; Rare:50 | ||||
chr3:69999524-69999755 | Rare:69 |