Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:42021882-42022031 | Common:5; Rare:30 | ||||
chr21:42524819-42525035 | Common:1; Rare:48 | ||||
chr21:46213484-46213751 | Rare:63 | ||||
chr22:17943643-17943852 | Rare:34 | ||||
chr22:18970338-18970570 | Common:5; Rare:76 | ||||
chr22:19171574-19171724 | Rare:57 | ||||
chr22:19176576-19176865 | Common:1; Rare:103; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr22:20081143-20081307 | Common:1; Rare:44 | ||||
chr22:20319174-20319389 | Common:1; Rare:40 | ||||
chr22:20656930-20657224 | Common:3; Rare:79 | ||||
chr22:20918102-20918139 | Rare:13 | ||||
chr22:21014151-21014473 | Rare:85 | ||||
chr22:22294072-22294208 | Common:1; Rare:22 | ||||
chr22:22298028-22298253 | Common:6; Rare:94 | ||||
chr22:23181717-23181772 | Rare:26 |