Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:28737660-28737766 | Rare:43 | ||||
chr1:31296744-31297120 | Common:5; Rare:119 | ||||
chr1:32179615-32179768 | Rare:32 | ||||
chr1:32291952-32292151 | Rare:74 | ||||
chr1:32394419-32394656 | Common:1; Rare:63 | ||||
chr1:32650924-32651313 | Common:2; Rare:150 | ||||
chr1:32817288-32817755 | Common:1; Rare:120; Clinvar:5; Clinvar (benign):3 | ||||
chr1:34166916-34167027 | Common:1; Rare:25 | ||||
chr1:35031711-35031791 | Rare:25 | ||||
chr1:35557369-35557460 | Rare:20 | ||||
chr1:35557622-35557837 | Common:2; Rare:80 | ||||
chr1:35641444-35641611 | Rare:37 | ||||
chr1:35769925-35770098 | Rare:43 | ||||
chr1:36088710-36088922 | Common:1; Rare:75 | ||||
chr1:36397886-36398008 | Common:2; Rare:28 |