Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32394403-32394690 | Common:1; Rare:81 | ||||
chr1:32464939-32465085 | Rare:47 | ||||
chr1:32539314-32539461 | Rare:28 | ||||
chr1:32650449-32650657 | Common:1; Rare:92 | ||||
chr1:32650918-32651322 | Common:2; Rare:150 | ||||
chr1:32817270-32817844 | Common:1; Rare:150; Clinvar:5; Clinvar (benign):4 | ||||
chr1:32818061-32818314 | Common:1; Rare:72 | ||||
chr1:32872445-32872615 | Rare:35 | ||||
chr1:33036802-33037105 | Rare:114; Clinvar (pathogenic):2 | ||||
chr1:33080985-33081165 | Common:2; Rare:44 | ||||
chr1:33392769-33393056 | Rare:43 | ||||
chr1:33472349-33472673 | Common:1; Rare:73 | ||||
chr1:33819813-33820102 | Rare:77 | ||||
chr1:34859709-34859912 | Common:1; Rare:56 | ||||
chr1:34985295-34985362 | Common:1; Rare:28 |