Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161045878-161046064 | Common:1; Rare:48 | ||||
chr1:161098289-161098404 | Common:1; Rare:18 | ||||
chr1:161118012-161118134 | Rare:56 | ||||
chr1:161132417-161132705 | Common:1; Rare:95 | ||||
chr1:161153732-161153799 | Rare:18 | ||||
chr1:161159392-161159507 | Common:1; Rare:29 | ||||
chr1:161166263-161166512 | Common:2; Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161225797-161226063 | Common:9; Rare:38 | ||||
chr1:161314267-161314412 | Common:3; Rare:54; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161367866-161367933 | Rare:17 | ||||
chr1:161749623-161749835 | Rare:72 | ||||
chr1:161766147-161766363 | Common:3; Rare:64 | ||||
chr1:162497741-162497855 | Common:1; Rare:32 | ||||
chr1:162790578-162790789 | Common:4; Rare:62 | ||||
chr1:163321705-163322057 | Common:1; Rare:96 |