Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:42615066-42615133 | Rare:11 | ||||
chr21:46122144-46122168 | Rare:10; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr22:17266632-17266795 | Rare:35 | ||||
chr22:21014175-21014403 | Rare:60 | ||||
chr22:21674994-21675109 | Rare:39 | ||||
chr22:22298026-22298221 | Common:6; Rare:88 | ||||
chr22:22686539-22686736 | Common:1; Rare:43 | ||||
chr22:23536652-23536878 | Common:1; Rare:52 | ||||
chr22:25447973-25448152 | Common:4; Rare:66 | ||||
chr22:26672658-26672959 | Common:2; Rare:75 | ||||
chr22:26672961-26673104 | Common:1; Rare:49 | ||||
chr22:28796125-28796250 | Rare:35 | ||||
chr22:30922233-30922339 | Rare:48 | ||||
chr22:30969023-30969292 | Common:2; Rare:76 | ||||
chr22:33573554-33573854 | Common:1; Rare:56 |