Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161132417-161132705 | Common:1; Rare:95 | ||||
chr1:161159365-161159523 | Common:2; Rare:44 | ||||
chr1:161166268-161166512 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161172251-161172466 | Common:1; Rare:52 | ||||
chr1:161199053-161199307 | Rare:41 | ||||
chr1:161223337-161223734 | Common:1; Rare:100; Clinvar:2 | ||||
chr1:161225741-161226087 | Common:10; Rare:51 | ||||
chr1:161238165-161238409 | Common:1; Rare:36 | ||||
chr1:161258553-161258782 | Common:2; Rare:52 | ||||
chr1:161314265-161314434 | Common:3; Rare:69; Clinvar:10; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161367836-161367890 | Rare:14 | ||||
chr1:161549789-161549893 | Rare:37 | ||||
chr1:161749796-161749850 | Rare:27 | ||||
chr1:161766153-161766382 | Common:3; Rare:73 | ||||
chr1:162381531-162381748 | Common:3; Rare:46 |