Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:238060732-238061057 | Common:4; Rare:102 | ||||
chr2:238203583-238203797 | Common:3; Rare:88 | ||||
chr2:238426655-238426980 | Common:6; Rare:82 | ||||
chr2:239401644-239401750 | Rare:50 | ||||
chr2:240025282-240025515 | Common:2; Rare:100; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr2:240557928-240558138 | Rare:70 | ||||
chr2:240560766-240560873 | Common:1; Rare:46 | ||||
chr2:241102263-241102360 | Common:2; Rare:40 | ||||
chr2:241149429-241149640 | Common:3; Rare:68 | ||||
chr2:241230153-241230394 | Rare:62 | ||||
chr2:241242656-241242906 | Common:3; Rare:53 | ||||
chr2:241248273-241248604 | Common:2; Rare:71 | ||||
chr2:241255467-241255844 | Rare:75 | ||||
chr2:241315109-241315406 | Common:5; Rare:100 | ||||
chr2:241315649-241316195 | Common:5; Rare:198 |