Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:33036772-33037079 | Common:1; Rare:121; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:33080992-33081165 | Common:2; Rare:43 | ||||
chr1:34985268-34985380 | Common:1; Rare:43 | ||||
chr1:35079322-35079422 | Common:3; Rare:30 | ||||
chr1:35192400-35192693 | Common:2; Rare:85 | ||||
chr1:35192697-35192742 | Common:1; Rare:20 | ||||
chr1:35557332-35557456 | Rare:34 | ||||
chr1:35557607-35557857 | Common:2; Rare:96 | ||||
chr1:35641340-35641404 | Rare:16 | ||||
chr1:35641479-35641626 | Rare:31 | ||||
chr1:35718820-35718895 | Rare:33 | ||||
chr1:36149420-36149800 | Common:2; Rare:107 | ||||
chr1:36224111-36224499 | Common:1; Rare:122 | ||||
chr1:36464146-36464503 | Common:3; Rare:118 | ||||
chr1:36475540-36475840 | Common:1; Rare:83; Clinvar:4; Clinvar (benign):2 |