Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:127343346-127343411 | Rare:8 | ||||
chr6:128520564-128520774 | Common:1; Rare:77 | ||||
chr6:130366200-130366421 | Common:3; Rare:45 | ||||
chr6:131628228-131628461 | Common:2; Rare:62 | ||||
chr6:132401428-132401589 | Common:1; Rare:48 | ||||
chr6:132814313-132814582 | Common:3; Rare:89 | ||||
chr6:134174859-134174963 | Rare:38 | ||||
chr6:134175674-134175963 | Common:2; Rare:70 | ||||
chr6:135497712-135497797 | Common:3; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
chr6:136289779-136290020 | Common:1; Rare:104 | ||||
chr6:137219356-137219456 | Common:2; Rare:34; Clinvar (benign):2 | ||||
chr6:138773654-138773785 | Common:1; Rare:61 | ||||
chr6:142147169-142147285 | Rare:43 | ||||
chr6:143060735-143060921 | Common:7; Rare:65 | ||||
chr6:143450651-143450927 | Common:1; Rare:104; Clinvar:4; Clinvar (benign):1 |