Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:45075507-45075778 | Common:3; Rare:57 | ||||
chr21:45076279-45076342 | Rare:12 | ||||
chr21:45077885-45078031 | Common:2; Rare:35 | ||||
chr21:45155718-45155947 | Common:2; Rare:16 | ||||
chr21:45182429-45182665 | Common:1; Rare:45 | ||||
chr21:45292134-45292352 | Common:2; Rare:80 | ||||
chr21:45295436-45295564 | Rare:34 | ||||
chr21:45296161-45296276 | Rare:18 | ||||
chr21:45364549-45364815 | Common:3; Rare:39 | ||||
chr21:45367089-45367308 | Common:5; Rare:53 | ||||
chr21:45412226-45412398 | Common:6; Rare:42 | ||||
chr21:45989575-45989652 | Common:2; Rare:28; Clinvar:1; Clinvar (benign):3 | ||||
chr21:45998116-45998433 | Common:1; Rare:110; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr21:46003129-46003674 | Common:7; Rare:209; Clinvar:27; Clinvar (benign):23 | ||||
chr21:46036369-46036512 | Common:3; Rare:28 |