Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32222288-32222462 | Rare:83 | ||||
chr1:32336231-32336323 | Rare:37 | ||||
chr1:32394402-32394656 | Common:1; Rare:70 | ||||
chr1:32464753-32465101 | Rare:83 | ||||
chr1:32650891-32651334 | Common:2; Rare:161 | ||||
chr1:32817289-32817695 | Common:1; Rare:102; Clinvar:5; Clinvar (benign):2 | ||||
chr1:32885774-32886011 | Rare:25 | ||||
chr1:32886269-32886508 | Rare:61 | ||||
chr1:33036806-33037067 | Rare:103; Clinvar (pathogenic):1 | ||||
chr1:33080992-33081203 | Common:2; Rare:63 | ||||
chr1:35031719-35032046 | Common:1; Rare:91 | ||||
chr1:35079284-35079422 | Common:3; Rare:36 | ||||
chr1:35193115-35193163 | Rare:24 | ||||
chr1:35557353-35557460 | Rare:29 | ||||
chr1:35557635-35557916 | Common:2; Rare:107 |