Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:208025475-208025619 | Common:1; Rare:38 | ||||
chr2:208255064-208255234 | Common:2; Rare:45 | ||||
chr2:208266131-208266306 | Common:6; Rare:64; Clinvar:1; Clinvar (benign):2 | ||||
chr2:210002423-210002670 | Common:6; Rare:87 | ||||
chr2:213284238-213284480 | Rare:76 | ||||
chr2:215311910-215312133 | Common:8; Rare:93 | ||||
chr2:216498689-216498886 | Common:6; Rare:80 | ||||
chr2:218217105-218217226 | Rare:50 | ||||
chr2:218270091-218270559 | Common:5; Rare:148; Clinvar:4; Clinvar (benign):1 | ||||
chr2:218568276-218568598 | Common:2; Rare:88 | ||||
chr2:218659500-218659767 | Common:1; Rare:69 | ||||
chr2:218671977-218672062 | Rare:29 | ||||
chr2:219176922-219177109 | Common:4; Rare:58 | ||||
chr2:219206683-219206909 | Rare:86 | ||||
chr2:219229606-219229905 | Common:1; Rare:83 |