Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:231420987-231421515 | Common:2; Rare:166; Clinvar:6; Clinvar (benign):5 | ||||
chr1:231422669-231422804 | Rare:34; Clinvar:2; Clinvar (benign):1 | ||||
chr1:231442891-231443135 | Common:1; Rare:46 | ||||
chr1:231501269-231501439 | Common:1; Rare:23 | ||||
chr1:244970970-244971080 | Rare:25 | ||||
chr1:246569747-246569935 | Common:1; Rare:33 | ||||
chr10:6140607-6140766 | Common:1; Rare:41 | ||||
chr10:6141231-6141283 | Rare:10 | ||||
chr10:6141285-6141321 | Rare:5 | ||||
chr10:6141502-6141824 | Common:2; Rare:71 | ||||
chr10:6163640-6163869 | Common:6; Rare:78 | ||||
chr10:6175478-6175754 | Common:6; Rare:48 | ||||
chr10:6177831-6177948 | Common:1; Rare:24 | ||||
chr10:6200603-6200944 | Common:8; Rare:69 | ||||
chr10:13118184-13118471 | Common:2; Rare:51 |