Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:36346301-36346787 | Common:7; Rare:132; Clinvar:3; Clinvar (benign):2 | ||||
chr13:36999296-36999459 | Rare:61 | ||||
chr13:37000259-37000397 | Common:2; Rare:24 | ||||
chr13:37000715-37000815 | Rare:43; Clinvar (pathogenic):1 | ||||
chr13:37059585-37059754 | Common:1; Rare:55 | ||||
chr13:38349522-38349911 | Common:4; Rare:129; Clinvar (pathogenic):1 | ||||
chr13:39038059-39038433 | Common:1; Rare:93 | ||||
chr13:39655559-39655803 | Common:4; Rare:122; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr13:40771078-40771373 | Common:3; Rare:106 | ||||
chr13:40789377-40789621 | Common:2; Rare:81; Clinvar:5; Clinvar (benign):2 | ||||
chr13:41061387-41061657 | Common:2; Rare:81 | ||||
chr13:41263525-41263601 | Rare:19 | ||||
chr13:42271794-42272190 | Common:4; Rare:105 | ||||
chr13:43023512-43023724 | Common:1; Rare:87 | ||||
chr13:43786874-43787165 | Rare:90 |