Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:45448748-45448893 | Common:2; Rare:35 | ||||
chr21:45469671-45470039 | Common:1; Rare:69 | ||||
chr21:45471814-45472034 | Rare:56 | ||||
chr21:45487161-45487466 | Common:5; Rare:99; Clinvar (benign):1 | ||||
chr21:46394497-46394738 | Rare:50 | ||||
chr22:19397062-19397297 | Common:2; Rare:40 | ||||
chr22:19603846-19604106 | Rare:48 | ||||
chr22:20287218-20287397 | Common:3; Rare:29 | ||||
chr22:20918133-20918238 | Rare:25 | ||||
chr22:22098583-22098720 | Rare:31 | ||||
chr22:22298014-22298196 | Common:9; Rare:84 | ||||
chr22:22686603-22686734 | Common:1; Rare:25 | ||||
chr22:23684717-23684823 | Rare:18 | ||||
chr22:25111528-25111965 | Common:5; Rare:71 | ||||
chr22:25112306-25112595 | Common:2; Rare:65 |