Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:36112322-36112336 | Rare:1 | ||||
chr20:40686316-40686577 | Common:1; Rare:48; Clinvar (benign):3 | ||||
chr20:41123020-41123310 | Common:1; Rare:42 | ||||
chr20:50172320-50172422 | Common:1; Rare:31 | ||||
chr20:50624488-50624798 | Common:2; Rare:62 | ||||
chr20:52973076-52973301 | Common:1; Rare:58 | ||||
chr20:57189912-57190149 | Common:3; Rare:34 | ||||
chr20:57264206-57264373 | Common:1; Rare:29 | ||||
chr20:58850890-58850923 | Rare:7 | ||||
chr20:58905275-58905444 | Common:2; Rare:33; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr20:62306039-62306317 | Common:1; Rare:80 | ||||
chr21:15063914-15063957 | Common:1; Rare:8 | ||||
chr21:16194263-16194599 | Common:2; Rare:93 | ||||
chr21:26964567-26964750 | Common:1; Rare:36 | ||||
chr21:26967034-26967121 | Rare:26 |