Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:234373419-234373775 | Common:1; Rare:167; Clinvar (benign):7 | ||||
chr1:234608020-234608197 | Common:1; Rare:55 | ||||
chr1:234608198-234608267 | Rare:24 | ||||
chr1:235128714-235129082 | Common:1; Rare:158 | ||||
chr1:235327825-235328073 | Rare:69 | ||||
chr1:235328116-235328409 | Common:2; Rare:85 | ||||
chr1:235328427-235328611 | Common:2; Rare:62 | ||||
chr1:235866847-235867142 | Common:3; Rare:87 | ||||
chr1:236064966-236065367 | Common:4; Rare:141; Clinvar (pathogenic):1 | ||||
chr1:236281925-236282295 | Common:6; Rare:106 | ||||
chr1:236395311-236395489 | Rare:44 | ||||
chr1:236523833-236524060 | Common:3; Rare:59 | ||||
chr1:236524532-236524625 | Common:1; Rare:19 | ||||
chr1:236604453-236604616 | Common:4; Rare:53 | ||||
chr1:241848121-241848224 | Rare:20 |