Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:44873506-44873542 | Rare:12 | ||||
chr21:44873549-44874094 | Common:9; Rare:205 | ||||
chr21:44939899-44940060 | Common:2; Rare:46 | ||||
chr21:45074470-45074787 | Common:3; Rare:149 | ||||
chr21:45287879-45288102 | Common:5; Rare:85 | ||||
chr21:45404885-45405222 | Common:13; Rare:187 | ||||
chr21:45542412-45542533 | Rare:37 | ||||
chr21:45981500-45981946 | Common:24; Rare:119; Clinvar:5; Clinvar (benign):4 | ||||
chr21:45986523-45987175 | Common:7; Rare:225; Clinvar:31; Clinvar (benign):15 | ||||
chr21:46000542-46000717 | Common:7; Rare:55 | ||||
chr21:46184470-46184773 | Common:1; Rare:18 | ||||
chr21:46229039-46229244 | Common:4; Rare:36 | ||||
chr21:46286222-46286402 | Common:4; Rare:67 | ||||
chr21:46323841-46324224 | Common:3; Rare:140; Clinvar:3; Clinvar (benign):2 | ||||
chr21:46458680-46459063 | Common:3; Rare:131 |