Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:37072991-37073390 | Common:5; Rare:152 | ||||
chr21:37366018-37366099 | Rare:26 | ||||
chr21:39380379-39380487 | Rare:49 | ||||
chr21:39445757-39445913 | Common:3; Rare:50 | ||||
chr21:42893073-42893336 | Common:3; Rare:87 | ||||
chr21:43659461-43659585 | Common:1; Rare:41 | ||||
chr21:43776239-43776388 | Common:2; Rare:59; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
chr21:44339226-44339443 | Common:2; Rare:68 | ||||
chr21:44873612-44874040 | Common:8; Rare:173 | ||||
chr21:45287867-45288102 | Common:6; Rare:92 | ||||
chr21:45981531-45981859 | Common:24; Rare:83; Clinvar:2; Clinvar (benign):3 | ||||
chr21:46002046-46002347 | Common:1; Rare:103; Clinvar:12; Clinvar (benign):11 | ||||
chr21:46286023-46286399 | Common:5; Rare:119 | ||||
chr21:46323841-46324203 | Common:2; Rare:126; Clinvar:2; Clinvar (benign):1 | ||||
chr22:17159197-17159365 | Common:4; Rare:78 |