Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:87155303-87155588 | Rare:77 | ||||
chr6:87589962-87590160 | Common:2; Rare:83; Clinvar (benign):4 | ||||
chr6:88963591-88963830 | Common:2; Rare:81 | ||||
chr6:89638722-89638758 | Rare:13 | ||||
chr6:90587033-90587334 | Common:2; Rare:76 | ||||
chr6:95577439-95577543 | Common:3; Rare:25 | ||||
chr6:96521723-96521856 | Common:3; Rare:61 | ||||
chr6:100881279-100881479 | Common:5; Rare:88 | ||||
chr6:106629462-106629640 | Common:3; Rare:39 | ||||
chr6:107459558-107459729 | Common:2; Rare:39 | ||||
chr6:107958131-107958416 | Common:1; Rare:87; Clinvar:2; Clinvar (benign):2 | ||||
chr6:108260914-108261153 | Rare:105 | ||||
chr6:109382416-109382806 | Common:5; Rare:116; Clinvar (benign):1 | ||||
chr6:109691181-109691315 | Common:1; Rare:31; Clinvar:4; Clinvar (benign):1 | ||||
chr6:110874667-110874785 | Common:3; Rare:34 |