Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:38012439-38012808 | Common:1; Rare:113 | ||||
chr1:38873301-38873554 | Common:3; Rare:87 | ||||
chr1:39025981-39026157 | Rare:27 | ||||
chr1:39026228-39026402 | Common:1; Rare:45 | ||||
chr1:39204575-39204863 | Rare:48 | ||||
chr1:39738766-39738927 | Common:1; Rare:39 | ||||
chr1:39883447-39883575 | Common:1; Rare:54; Clinvar (pathogenic):1 | ||||
chr1:40040433-40040812 | Common:3; Rare:118 | ||||
chr1:40161215-40161415 | Common:1; Rare:56 | ||||
chr1:40257909-40258303 | Common:4; Rare:107; Clinvar:7; Clinvar (benign):1 | ||||
chr1:40449958-40450182 | Common:4; Rare:85 | ||||
chr1:40508653-40508789 | Common:3; Rare:36 | ||||
chr1:40531509-40531725 | Common:1; Rare:56 | ||||
chr1:40691517-40691860 | Common:2; Rare:155 | ||||
chr1:40692039-40692292 | Common:1; Rare:78 |