Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:45349834-45350132 | Common:2; Rare:55 | ||||
chr21:45590527-45590785 | Common:6; Rare:88 | ||||
chr22:17733591-17733656 | Rare:10 | ||||
chr22:18056925-18057048 | Rare:24 | ||||
chr22:19176463-19176586 | Rare:61; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr22:20131049-20131283 | Common:5; Rare:92 | ||||
chr22:22298040-22298196 | Common:2; Rare:67 | ||||
chr22:22369488-22369617 | Common:1; Rare:37 | ||||
chr22:22380530-22380865 | Common:3; Rare:106 | ||||
chr22:22720458-22720629 | Common:2; Rare:39 | ||||
chr22:22822659-22822822 | Common:1; Rare:66 | ||||
chr22:22901005-22901099 | Rare:31 | ||||
chr22:25447990-25448136 | Common:3; Rare:48 | ||||
chr22:26672639-26672816 | Common:2; Rare:42 | ||||
chr22:29481780-29481945 | Rare:31 |