Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:58326875-58327021 | Common:1; Rare:31 | ||||
chr19:58347605-58347774 | Common:7; Rare:80 | ||||
chr19:58499194-58499545 | Common:3; Rare:116; Clinvar:4; Clinvar (benign):2 | ||||
chr2:677376-677728 | Common:3; Rare:117 | ||||
chr2:3558269-3558695 | Common:6; Rare:151 | ||||
chr2:3575107-3575373 | Common:2; Rare:82; Clinvar:3; Clinvar (benign):6 | ||||
chr2:9423443-9423677 | Rare:73 | ||||
chr2:9555729-9555992 | Common:2; Rare:87 | ||||
chr2:9630950-9631316 | Common:3; Rare:118 | ||||
chr2:9843250-9843501 | Common:6; Rare:70 | ||||
chr2:10689934-10690014 | Common:2; Rare:26 | ||||
chr2:12716629-12716965 | Common:3; Rare:102 | ||||
chr2:15561297-15561415 | Rare:47 | ||||
chr2:17753738-17754125 | Common:3; Rare:122 | ||||
chr2:19901664-19901792 | Common:1; Rare:70 |