Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:32372819-32372945 | Rare:18 | ||||
chr21:32569464-32569743 | Common:2; Rare:50 | ||||
chr21:33945808-33945890 | Common:1; Rare:7 | ||||
chr21:36005185-36005323 | Rare:25 | ||||
chr21:36135560-36135716 | Common:2; Rare:32 | ||||
chr21:38907266-38907475 | Rare:39 | ||||
chr21:45992188-45992397 | Common:1; Rare:71; Clinvar:8; Clinvar (benign):3 | ||||
chr21:46130376-46130439 | Rare:21 | ||||
chr22:22298035-22298197 | Common:4; Rare:72 | ||||
chr22:25447980-25448131 | Common:3; Rare:50 | ||||
chr22:26672644-26672959 | Common:2; Rare:79 | ||||
chr22:30922233-30922339 | Rare:48 | ||||
chr22:31454394-31454427 | Rare:9 | ||||
chr22:36288783-36289135 | Common:2; Rare:98; Clinvar:2; Clinvar (benign):4 | ||||
chr22:36331578-36331733 | Common:2; Rare:25 |