Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:19757512-19757706 | Common:3; Rare:55 | ||||
chr20:19757946-19758276 | Common:4; Rare:114 | ||||
chr20:32475274-32475606 | Common:1; Rare:77 | ||||
chr20:33812304-33812395 | Rare:11 | ||||
chr20:35490932-35491051 | Rare:23 | ||||
chr20:36050045-36050163 | Common:1; Rare:28 | ||||
chr20:36050274-36050645 | Common:2; Rare:122 | ||||
chr20:41116014-41116339 | Common:1; Rare:60; Clinvar (pathogenic):1 | ||||
chr20:44904768-44905064 | Rare:48 | ||||
chr20:45419362-45419533 | Common:1; Rare:71; Clinvar (pathogenic):1 | ||||
chr20:62306371-62306725 | Common:3; Rare:131 | ||||
chr21:25561838-25562129 | Common:1; Rare:82 | ||||
chr21:33945808-33945857 | Rare:5 | ||||
chr21:36430083-36430389 | Common:3; Rare:61 | ||||
chr21:38503533-38503871 | Common:3; Rare:64 |