Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:9423457-9423709 | Rare:85 | ||||
chr2:9474504-9474592 | Common:6; Rare:49 | ||||
chr2:9843391-9843434 | Common:2; Rare:10 | ||||
chr2:10812704-10813020 | Common:3; Rare:119 | ||||
chr2:17753706-17753866 | Common:1; Rare:57 | ||||
chr2:19990102-19990229 | Rare:34 | ||||
chr2:20446881-20447091 | Common:2; Rare:78 | ||||
chr2:20651059-20651276 | Rare:71 | ||||
chr2:20823064-20823159 | Rare:36 | ||||
chr2:23927067-23927273 | Common:2; Rare:75 | ||||
chr2:23940354-23940481 | Common:3; Rare:37 | ||||
chr2:24076273-24076594 | Rare:84 | ||||
chr2:26033859-26034143 | Common:1; Rare:89 | ||||
chr2:26244602-26244965 | Common:2; Rare:131; Clinvar:5; Clinvar (benign):7 | ||||
chr2:26345829-26346132 | Common:1; Rare:80 |