Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:128791307-128791463 | Common:1; Rare:44 | ||||
chr7:129611662-129611790 | Common:1; Rare:44 | ||||
chr7:131109888-131110123 | Common:1; Rare:41 | ||||
chr7:131327711-131327912 | Rare:67 | ||||
chr7:135148020-135148122 | Rare:27 | ||||
chr7:135170666-135170816 | Common:2; Rare:60 | ||||
chr7:136869084-136869264 | Common:1; Rare:42; Clinvar (benign):2 | ||||
chr7:139109341-139109464 | Common:1; Rare:37 | ||||
chr7:140696810-140696829 | Rare:7 | ||||
chr7:141738228-141738428 | Rare:84 | ||||
chr7:143381024-143381397 | Common:1; Rare:127 | ||||
chr7:149028641-149028969 | Common:1; Rare:106 | ||||
chr7:149126274-149126427 | Common:5; Rare:49 | ||||
chr7:149261961-149262208 | Common:2; Rare:83 | ||||
chr7:151063104-151063165 | Rare:22 |