Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:31296744-31297086 | Common:5; Rare:112 | ||||
chr1:32291870-32292151 | Common:1; Rare:89 | ||||
chr1:32650989-32651218 | Common:1; Rare:73 | ||||
chr1:32817270-32817571 | Rare:74; Clinvar:4 | ||||
chr1:33036824-33037104 | Rare:102; Clinvar (pathogenic):1 | ||||
chr1:35557376-35557456 | Rare:16 | ||||
chr1:35557597-35557837 | Common:2; Rare:89 | ||||
chr1:36224103-36224459 | Common:1; Rare:102 | ||||
chr1:37474395-37474581 | Common:1; Rare:74 | ||||
chr1:37690510-37690731 | Common:5; Rare:53 | ||||
chr1:37692238-37692569 | Common:4; Rare:77 | ||||
chr1:38873307-38873564 | Common:3; Rare:91 | ||||
chr1:40040444-40040788 | Common:3; Rare:102 | ||||
chr1:40257915-40258274 | Common:4; Rare:98; Clinvar:7 | ||||
chr1:42335216-42335417 | Common:5; Rare:92 |