Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:173856702-173857014 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
chr1:173857561-173857810 | Rare:56; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr1:173859408-173859434 | Rare:5 | ||||
chr1:173859742-173860054 | Common:3; Rare:52 | ||||
chr1:173860309-173860491 | Common:1; Rare:26 | ||||
chr1:173860908-173860980 | Rare:13 | ||||
chr1:173861030-173861301 | Common:4; Rare:57 | ||||
chr1:173862687-173862862 | Common:4; Rare:52 | ||||
chr1:173863437-173863474 | Rare:6 | ||||
chr1:173864187-173864475 | Rare:103 | ||||
chr1:173865390-173865442 | Rare:16 | ||||
chr1:173866922-173867434 | Common:6; Rare:149 | ||||
chr1:173928742-173928877 | Common:1; Rare:18 | ||||
chr1:173946496-173946795 | Common:1; Rare:64 | ||||
chr1:174021614-174021771 | Rare:47 |