Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:127343344-127343568 | Common:1; Rare:46 | ||||
chr6:127343578-127343639 | Common:1; Rare:16 | ||||
chr6:128520463-128520763 | Common:2; Rare:97 | ||||
chr6:131628095-131628461 | Common:3; Rare:95 | ||||
chr6:132401435-132401595 | Common:1; Rare:46 | ||||
chr6:133953044-133953242 | Common:2; Rare:61 | ||||
chr6:134174824-134175025 | Common:1; Rare:105 | ||||
chr6:135497618-135497817 | Common:4; Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
chr6:136289769-136290014 | Common:1; Rare:106 | ||||
chr6:136550372-136550669 | Common:2; Rare:91 | ||||
chr6:137044710-137044756 | Rare:7 | ||||
chr6:137044922-137044992 | Rare:23 | ||||
chr6:137866941-137867233 | Rare:66 | ||||
chr6:138107102-138107485 | Common:3; Rare:126 | ||||
chr6:138107803-138107821 | Rare:4 |