Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:44188935-44189095 | Rare:30 | ||||
chr20:45424261-45424561 | Common:3; Rare:80; Clinvar (pathogenic):1 | ||||
chr20:47317356-47317572 | Common:1; Rare:43 | ||||
chr20:47352505-47352632 | Rare:21 | ||||
chr20:47357784-47357824 | Rare:8 | ||||
chr20:47358856-47358953 | Rare:19 | ||||
chr20:47658321-47658623 | Rare:69 | ||||
chr20:48025107-48025238 | Common:1; Rare:25 | ||||
chr20:49775369-49775603 | Common:2; Rare:40 | ||||
chr20:50267421-50267502 | Common:3; Rare:16 | ||||
chr20:58310641-58310689 | Rare:8 | ||||
chr20:62306454-62306733 | Common:2; Rare:100 | ||||
chr20:62307155-62307447 | Common:1; Rare:91 | ||||
chr20:62307565-62307617 | Rare:29 | ||||
chr20:62378806-62378899 | Common:1; Rare:21 |