Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:140107679-140107846 | Rare:57 | ||||
chr5:140346593-140346682 | Rare:26 | ||||
chr5:140564556-140564837 | Rare:74 | ||||
chr5:140647583-140647924 | Common:5; Rare:139; Clinvar:4; Clinvar (benign):3 | ||||
chr5:140691300-140691633 | Common:1; Rare:120; Clinvar:10; Clinvar (benign):1 | ||||
chr5:141320725-141320867 | Common:2; Rare:46 | ||||
chr5:141636810-141637011 | Common:2; Rare:86 | ||||
chr5:141651614-141651855 | Common:1; Rare:39 | ||||
chr5:141923750-141923868 | Common:1; Rare:22 | ||||
chr5:142325008-142325184 | Rare:59 | ||||
chr5:145937638-145937770 | Rare:32 | ||||
chr5:146182501-146182827 | Common:3; Rare:90 | ||||
chr5:147234930-147235125 | Rare:61 | ||||
chr5:148383777-148384021 | Rare:72 | ||||
chr5:149550870-149551056 | Rare:45 |