Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:90256519-90256600 | Common:1; Rare:32 | ||||
chr14:90396877-90397232 | Common:5; Rare:168; Clinvar (benign):2 | ||||
chr14:91113771-91114406 | Common:1; Rare:143 | ||||
chr14:91510258-91510706 | Common:1; Rare:153 | ||||
chr14:91836421-91836681 | Common:12; Rare:44 | ||||
chr14:91946975-91947137 | Common:1; Rare:23 | ||||
chr14:92040008-92040159 | Common:3; Rare:45; Clinvar:3; Clinvar (benign):2 | ||||
chr14:92121649-92122005 | Common:5; Rare:123 | ||||
chr14:92748596-92748769 | Rare:46 | ||||
chr14:92794004-92794375 | Rare:113 | ||||
chr14:93184845-93185017 | Rare:58 | ||||
chr14:93206992-93207294 | Common:2; Rare:150 | ||||
chr14:94081125-94081375 | Common:5; Rare:80 | ||||
chr14:95157424-95157690 | Common:4; Rare:94 | ||||
chr14:95534568-95534664 | Rare:41 |