Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:37072998-37073379 | Common:5; Rare:147 | ||||
chr21:37267290-37267651 | Common:3; Rare:128 | ||||
chr21:37267899-37268128 | Rare:63 | ||||
chr21:37366025-37366115 | Rare:26 | ||||
chr21:38498440-38498722 | Common:1; Rare:37 | ||||
chr21:39445729-39446081 | Common:4; Rare:105 | ||||
chr21:39451685-39452139 | Common:3; Rare:130 | ||||
chr21:41879320-41879586 | Common:5; Rare:83 | ||||
chr21:42514420-42514552 | Rare:29 | ||||
chr21:42879527-42879665 | Common:3; Rare:46 | ||||
chr21:42893088-42893378 | Common:3; Rare:105 | ||||
chr21:43659486-43659644 | Common:1; Rare:48 | ||||
chr21:43776229-43776491 | Common:5; Rare:95; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
chr21:43925235-43925403 | Common:1; Rare:26 | ||||
chr21:44339248-44339449 | Common:2; Rare:61 |