Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:31087770-31088114 | Common:3; Rare:102 | ||||
chr22:31088283-31088554 | Common:2; Rare:61 | ||||
chr22:31088560-31088969 | Common:1; Rare:117 | ||||
chr22:31093163-31093388 | Common:1; Rare:45 | ||||
chr22:31107381-31107765 | Common:2; Rare:119 | ||||
chr22:31290722-31290911 | Rare:76 | ||||
chr22:31292400-31292603 | Common:1; Rare:42 | ||||
chr22:31489739-31490195 | Common:4; Rare:181 | ||||
chr22:31496409-31496556 | Common:1; Rare:37 | ||||
chr22:31630809-31631038 | Common:5; Rare:54 | ||||
chr22:31662192-31662368 | Common:2; Rare:75 | ||||
chr22:31750031-31750344 | Common:3; Rare:93 | ||||
chr22:31753782-31753996 | Rare:80 | ||||
chr22:32474639-32475337 | Common:6; Rare:230; Clinvar:6; Clinvar (benign):3 | ||||
chr22:32801459-32801710 | Rare:71; Clinvar:3; Clinvar (benign):2 |