Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:37514736-37514878 | Common:3; Rare:87 | ||||
chr1:37595888-37596044 | Common:1; Rare:52 | ||||
chr1:37690433-37690768 | Common:7; Rare:98 | ||||
chr1:37692197-37692589 | Common:5; Rare:93 | ||||
chr1:37859575-37859804 | Common:4; Rare:77 | ||||
chr1:37946997-37947143 | Common:1; Rare:30 | ||||
chr1:37989954-37990193 | Rare:82 | ||||
chr1:38859720-38859951 | Rare:83 | ||||
chr1:38873301-38873554 | Common:3; Rare:87 | ||||
chr1:39026235-39026397 | Common:1; Rare:43 | ||||
chr1:39215001-39215277 | Rare:47 | ||||
chr1:39738757-39738903 | Common:1; Rare:27 | ||||
chr1:39883467-39883586 | Rare:45; Clinvar (pathogenic):1 | ||||
chr1:39954983-39955170 | Common:1; Rare:50 | ||||
chr1:40040444-40040801 | Common:3; Rare:108 |