Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:4723755-4723856 | Common:1; Rare:34 | ||||
chr19:4867626-4867855 | Common:3; Rare:68 | ||||
chr19:5293203-5293421 | Common:1; Rare:98 | ||||
chr19:5622681-5623313 | Common:6; Rare:255 | ||||
chr19:5680473-5680772 | Rare:90 | ||||
chr19:5680927-5681040 | Rare:29 | ||||
chr19:5790574-5790837 | Common:5; Rare:78 | ||||
chr19:5978078-5978213 | Common:3; Rare:51 | ||||
chr19:6333517-6333740 | Common:3; Rare:57 | ||||
chr19:6740819-6740907 | Rare:23 | ||||
chr19:7395014-7395240 | Common:6; Rare:65 | ||||
chr19:7535574-7535763 | Common:3; Rare:68 | ||||
chr19:7629525-7629849 | Common:5; Rare:116; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:7636969-7637167 | Common:2; Rare:62; Clinvar (benign):1 | ||||
chr19:7903542-7903912 | Rare:116 |