Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32964617-32964665 | Rare:13 | ||||
chr1:32964712-32965091 | Common:2; Rare:137 | ||||
chr1:33036791-33037184 | Rare:141; Clinvar (pathogenic):2 | ||||
chr1:33080936-33081196 | Common:2; Rare:73 | ||||
chr1:33182012-33182181 | Rare:38 | ||||
chr1:33256224-33256584 | Common:1; Rare:90 | ||||
chr1:33348982-33349235 | Rare:52 | ||||
chr1:33349753-33350197 | Common:3; Rare:144 | ||||
chr1:33472278-33472749 | Common:1; Rare:93 | ||||
chr1:34859655-34860003 | Common:1; Rare:88 | ||||
chr1:34985252-34985636 | Common:4; Rare:99 | ||||
chr1:35031181-35031294 | Rare:28 | ||||
chr1:35031587-35031845 | Common:1; Rare:81 | ||||
chr1:35031912-35032069 | Common:1; Rare:43 | ||||
chr1:35079271-35079605 | Common:3; Rare:80 |