Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39026228-39026389 | Common:1; Rare:40 | ||||
chr1:40040457-40040791 | Common:3; Rare:98 | ||||
chr1:40161276-40161394 | Rare:29 | ||||
chr1:40257941-40258264 | Common:4; Rare:85; Clinvar:7 | ||||
chr1:40508691-40508773 | Common:3; Rare:21 | ||||
chr1:42335164-42335430 | Common:5; Rare:124 | ||||
chr1:42456471-42456577 | Rare:49 | ||||
chr1:42658317-42658447 | Rare:38 | ||||
chr1:42767023-42767303 | Common:4; Rare:85 | ||||
chr1:42816961-42817134 | Common:1; Rare:49 | ||||
chr1:42846401-42846638 | Common:1; Rare:65 | ||||
chr1:42958858-42959070 | Common:1; Rare:58; Clinvar:4; Clinvar (benign):2 | ||||
chr1:43172228-43172335 | Common:1; Rare:57 | ||||
chr1:43270013-43270082 | Common:3; Rare:11 | ||||
chr1:43358690-43358986 | Common:7; Rare:91 |