Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179877743-179878006 | Rare:52 | ||||
chr1:179882201-179882437 | Rare:47 | ||||
chr1:179882493-179882950 | Common:1; Rare:230; Clinvar:9; Clinvar (benign):4 | ||||
chr1:179954669-179955314 | Common:3; Rare:139 | ||||
chr1:180502376-180502668 | Common:1; Rare:106 | ||||
chr1:181088494-181088711 | Rare:71 | ||||
chr1:182391286-182391483 | Rare:41 | ||||
chr1:182789620-182789810 | Common:2; Rare:71 | ||||
chr1:183635634-183636071 | Common:3; Rare:123 | ||||
chr1:184386728-184386886 | Common:3; Rare:50 | ||||
chr1:184386892-184387213 | Common:1; Rare:78 | ||||
chr1:184387224-184387368 | Rare:25 | ||||
chr1:184754589-184754682 | Common:1; Rare:44 | ||||
chr1:185156675-185157303 | Common:3; Rare:191 | ||||
chr1:185157420-185157527 | Common:1; Rare:35 |