Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:117929568-117929802 | Common:3; Rare:69 | ||||
chr1:119140645-119140748 | Rare:29 | ||||
chr1:120176432-120176535 | Rare:28 | ||||
chr1:145823922-145824238 | Rare:109 | ||||
chr1:145918700-145919013 | Common:2; Rare:64 | ||||
chr1:145927415-145927657 | Common:1; Rare:68; Clinvar (pathogenic):1 | ||||
chr1:145964587-145964748 | Rare:38 | ||||
chr1:147172427-147172744 | Common:1; Rare:85 | ||||
chr1:147225256-147225530 | Common:3; Rare:58 | ||||
chr1:147541205-147541518 | Common:2; Rare:48 | ||||
chr1:149886663-149886959 | Rare:100 | ||||
chr1:149887952-149888178 | Rare:52 | ||||
chr1:149927760-149927906 | Common:1; Rare:59; Clinvar (benign):4 | ||||
chr1:150067633-150067873 | Rare:71 | ||||
chr1:150293730-150293903 | Rare:60 |