Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39739284-39739340 | Rare:11 | ||||
chr1:39788761-39789088 | Common:3; Rare:107 | ||||
chr1:39883445-39883628 | Common:1; Rare:71; Clinvar (pathogenic):1 | ||||
chr1:39901776-39902126 | Common:6; Rare:112 | ||||
chr1:39954919-39955207 | Common:1; Rare:75 | ||||
chr1:40039801-40040235 | Common:3; Rare:94 | ||||
chr1:40040365-40040799 | Common:3; Rare:134 | ||||
chr1:40041277-40041466 | Rare:38 | ||||
chr1:40097181-40097407 | Common:2; Rare:85; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):5 | ||||
chr1:40161116-40161456 | Common:1; Rare:100 | ||||
chr1:40161598-40161722 | Common:1; Rare:33 | ||||
chr1:40161802-40161832 | Rare:8 | ||||
chr1:40247750-40247947 | Rare:32 | ||||
chr1:40257692-40258306 | Common:5; Rare:160; Clinvar:9; Clinvar (benign):1 | ||||
chr1:40373493-40373794 | Common:1; Rare:73 |