Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:108692523-108692896 | Common:3; Rare:134 | ||||
chr1:108746457-108746781 | Common:2; Rare:118 | ||||
chr1:108963362-108963563 | Common:1; Rare:77 | ||||
chr1:109075912-109076112 | Rare:76 | ||||
chr1:109090605-109090910 | Common:4; Rare:72 | ||||
chr1:109213848-109214129 | Rare:92 | ||||
chr1:109282894-109283197 | Common:2; Rare:51 | ||||
chr1:109397876-109398179 | Common:1; Rare:88 | ||||
chr1:109426285-109426791 | Common:3; Rare:158 | ||||
chr1:109483811-109484029 | Common:3; Rare:64 | ||||
chr1:109548496-109549065 | Common:6; Rare:175; Clinvar (pathogenic):1 | ||||
chr1:109616097-109616269 | Common:1; Rare:21 | ||||
chr1:109619747-109620059 | Common:1; Rare:58 | ||||
chr1:109620351-109620668 | Common:2; Rare:56 | ||||
chr1:109656139-109656368 | Common:1; Rare:47 |