Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:36104408-36104650 | Common:1; Rare:55 | ||||
chr21:36104722-36104977 | Common:3; Rare:54 | ||||
chr21:36320789-36320829 | Rare:17 | ||||
chr21:42917488-42917727 | Common:3; Rare:41 | ||||
chr21:42923853-42924156 | Common:1; Rare:58 | ||||
chr21:42925544-42925826 | Common:4; Rare:67 | ||||
chr21:42957081-42957322 | Common:2; Rare:47 | ||||
chr21:42975627-42975650 | Common:1; Rare:5 | ||||
chr21:45512084-45512210 | Common:1; Rare:50; Clinvar (benign):2 | ||||
chr22:17234160-17234175 | Rare:2 | ||||
chr22:22297940-22298206 | Common:13; Rare:111 | ||||
chr22:25447968-25448164 | Common:4; Rare:71 | ||||
chr22:26657204-26657639 | Common:2; Rare:97 | ||||
chr22:27742257-27742308 | Rare:5 | ||||
chr22:28799090-28799416 | Rare:57 |