Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32201596-32201733 | Rare:29 | ||||
chr1:32205453-32205668 | Common:3; Rare:68 | ||||
chr1:32222284-32222539 | Common:1; Rare:108 | ||||
chr1:32291909-32292156 | Common:1; Rare:83 | ||||
chr1:32336078-32336143 | Rare:19 | ||||
chr1:32336231-32336320 | Rare:36 | ||||
chr1:32351396-32351639 | Common:1; Rare:63 | ||||
chr1:32394403-32394680 | Common:1; Rare:78 | ||||
chr1:32464764-32465101 | Rare:79 | ||||
chr1:32650881-32651318 | Common:2; Rare:160 | ||||
chr1:32753823-32754026 | Common:2; Rare:71 | ||||
chr1:32817266-32817832 | Common:1; Rare:151; Clinvar:5; Clinvar (benign):4 | ||||
chr1:33036826-33037104 | Rare:101; Clinvar (pathogenic):1 | ||||
chr1:33080992-33081174 | Common:2; Rare:45 | ||||
chr1:33472349-33472668 | Common:1; Rare:73 |