Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32650525-32650657 | Common:1; Rare:59 | ||||
chr1:32650927-32651322 | Common:2; Rare:149 | ||||
chr1:32651715-32651968 | Rare:64 | ||||
chr1:32753856-32754156 | Common:2; Rare:106 | ||||
chr1:32817289-32817699 | Common:1; Rare:104; Clinvar:5; Clinvar (benign):2 | ||||
chr1:32895303-32895567 | Rare:88 | ||||
chr1:32895595-32895912 | Common:2; Rare:96 | ||||
chr1:32901312-32901534 | Common:1; Rare:50 | ||||
chr1:33036826-33037104 | Rare:101; Clinvar (pathogenic):1 | ||||
chr1:33080992-33081171 | Common:2; Rare:44 | ||||
chr1:35192714-35192733 | Common:1; Rare:10 | ||||
chr1:35268637-35269033 | Rare:140 | ||||
chr1:35557349-35557430 | Rare:26 | ||||
chr1:35557591-35557842 | Common:2; Rare:92 | ||||
chr1:35641472-35641639 | Common:1; Rare:38 |