Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32753856-32754041 | Common:1; Rare:67 | ||||
chr1:32765792-32766007 | Common:1; Rare:50 | ||||
chr1:32817237-32817750 | Common:1; Rare:139; Clinvar:5; Clinvar (benign):3 | ||||
chr1:33036826-33037105 | Rare:101; Clinvar (pathogenic):1 | ||||
chr1:33080983-33081203 | Common:2; Rare:65 | ||||
chr1:33182041-33182130 | Rare:22 | ||||
chr1:33392657-33393014 | Rare:46 | ||||
chr1:33430993-33431260 | Common:2; Rare:72 | ||||
chr1:33472349-33472678 | Common:1; Rare:73 | ||||
chr1:34165231-34165380 | Common:1; Rare:29 | ||||
chr1:35031638-35031783 | Common:1; Rare:48 | ||||
chr1:35031845-35032011 | Common:1; Rare:43 | ||||
chr1:35079317-35079434 | Common:3; Rare:34 | ||||
chr1:35192246-35192664 | Common:3; Rare:124 | ||||
chr1:35192687-35192793 | Common:4; Rare:58 |