Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32817308-32817694 | Common:1; Rare:101; Clinvar:5; Clinvar (benign):2 | ||||
chr1:33036814-33037108 | Rare:108; Clinvar (pathogenic):1 | ||||
chr1:33080992-33081158 | Common:2; Rare:38 | ||||
chr1:33472349-33472657 | Common:1; Rare:72 | ||||
chr1:35079210-35079422 | Common:3; Rare:54 | ||||
chr1:35193088-35193440 | Common:2; Rare:118 | ||||
chr1:35268862-35269037 | Rare:74 | ||||
chr1:35557376-35557486 | Common:1; Rare:24 | ||||
chr1:35557629-35557850 | Common:2; Rare:88 | ||||
chr1:35641464-35641620 | Rare:32 | ||||
chr1:35769919-35770098 | Rare:46 | ||||
chr1:36083995-36084128 | Common:3; Rare:47 | ||||
chr1:36088738-36088916 | Common:1; Rare:63 | ||||
chr1:36149420-36149778 | Common:2; Rare:102 | ||||
chr1:36224097-36224489 | Common:1; Rare:121 |