Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:46901714-46901824 | Common:3; Rare:20 | ||||
chr20:47352571-47352650 | Rare:13 | ||||
chr20:47357792-47357864 | Rare:14 | ||||
chr20:52727860-52728097 | Common:2; Rare:58 | ||||
chr20:53504295-53504409 | Common:2; Rare:44 | ||||
chr20:62307753-62308157 | Common:3; Rare:145 | ||||
chr20:62322306-62322634 | Common:5; Rare:109; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr20:62551490-62551640 | Common:1; Rare:38 | ||||
chr21:13515912-13516112 | Common:1; Rare:50 | ||||
chr21:21845001-21845291 | Common:3; Rare:73 | ||||
chr21:21909960-21910140 | Rare:65 | ||||
chr21:26967057-26967102 | Rare:15 | ||||
chr21:28539172-28539352 | Rare:26 | ||||
chr21:33868076-33868357 | Common:3; Rare:78 | ||||
chr21:37073825-37074028 | Common:2; Rare:45 |