Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:29002744-29002826 | Common:1; Rare:31 | ||||
chr21:38907266-38907475 | Rare:39 | ||||
chr21:44953854-44954040 | Rare:33 | ||||
chr21:45992187-45992390 | Common:1; Rare:70; Clinvar:8; Clinvar (benign):3 | ||||
chr22:19758631-19758770 | Rare:37 | ||||
chr22:19759328-19759448 | Common:1; Rare:32 | ||||
chr22:22298058-22298196 | Common:2; Rare:50 | ||||
chr22:22380701-22380833 | Common:1; Rare:44 | ||||
chr22:38336167-38336381 | Rare:64 | ||||
chr22:42600993-42601229 | Common:1; Rare:49 | ||||
chr22:46069842-46070051 | Rare:45 | ||||
chr3:16837763-16837943 | Common:1; Rare:33 | ||||
chr3:40453175-40453393 | Common:4; Rare:48 | ||||
chr3:42654389-42654619 | Rare:69 | ||||
chr3:75435081-75435388 | Common:4; Rare:105 |