Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:95233929-95234264 | Common:5; Rare:105 | ||||
chr1:95234686-95234775 | Common:1; Rare:25 | ||||
chr1:96721524-96721818 | Common:3; Rare:123 | ||||
chr1:97920887-97921163 | Rare:110; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr1:97921313-97921534 | Common:3; Rare:43 | ||||
chr1:98661479-98661899 | Common:4; Rare:142 | ||||
chr1:98662003-98662237 | Rare:54 | ||||
chr1:99766624-99766734 | Rare:22 | ||||
chr1:99849823-99850430 | Common:2; Rare:169; Clinvar:3; Clinvar (benign):2 | ||||
chr1:99969673-99969765 | Common:1; Rare:19 | ||||
chr1:99969818-99970092 | Rare:59 | ||||
chr1:99970353-99970525 | Rare:42 | ||||
chr1:100037897-100038336 | Common:2; Rare:153 | ||||
chr1:100038347-100038447 | Common:1; Rare:30 | ||||
chr1:100038490-100038924 | Common:5; Rare:144 |