Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:49512922-49513121 | Rare:44 | ||||
chr20:50379311-50379518 | Rare:53 | ||||
chr20:52973102-52973296 | Common:1; Rare:52 | ||||
chr20:63945652-63945883 | Rare:99 | ||||
chr21:16194157-16194612 | Common:3; Rare:124 | ||||
chr21:16419194-16419464 | Common:2; Rare:57 | ||||
chr21:25639792-25639816 | Rare:10 | ||||
chr21:26844328-26844608 | Common:2; Rare:107 | ||||
chr21:26964573-26964764 | Common:1; Rare:36 | ||||
chr21:26965555-26965606 | Rare:20 | ||||
chr21:26967086-26967123 | Rare:8 | ||||
chr21:26967142-26967254 | Rare:25 | ||||
chr21:29002719-29002826 | Common:1; Rare:38 | ||||
chr21:29076794-29076948 | Common:1; Rare:34 | ||||
chr21:31667165-31667274 | Rare:22; Clinvar (pathogenic):2 |