Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:40998164-40998428 | Rare:36 | ||||
chr6:41590037-41590305 | Common:1; Rare:85 | ||||
chr6:42658025-42658314 | Common:1; Rare:86 | ||||
chr6:42787355-42787383 | Rare:5 | ||||
chr6:42935815-42936102 | Common:3; Rare:57 | ||||
chr6:43038282-43038615 | Rare:101; Clinvar:4; Clinvar (pathogenic):1 | ||||
chr6:43998654-43998868 | Common:2; Rare:34 | ||||
chr6:44074646-44074735 | Rare:15 | ||||
chr6:44142778-44142880 | Rare:21 | ||||
chr6:44250093-44250195 | Common:1; Rare:34 | ||||
chr6:44251095-44251429 | Common:2; Rare:103 | ||||
chr6:44253270-44253663 | Common:6; Rare:163 | ||||
chr6:52420877-52421027 | Rare:30 | ||||
chr6:53509579-53509608 | Rare:6 | ||||
chr6:56800742-56801019 | Common:4; Rare:60 |