Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:140564573-140564838 | Rare:73 | ||||
chr5:140647579-140647889 | Common:5; Rare:126; Clinvar:4; Clinvar (benign):3 | ||||
chr5:140691305-140691661 | Common:1; Rare:130; Clinvar:11; Clinvar (benign):2 | ||||
chr5:141320732-141321004 | Common:3; Rare:87 | ||||
chr5:141636797-141637012 | Common:2; Rare:100 | ||||
chr5:141680820-141681114 | Common:1; Rare:56 | ||||
chr5:141682187-141682328 | Common:1; Rare:47 | ||||
chr5:141923553-141923910 | Common:1; Rare:97 | ||||
chr5:142324973-142325236 | Rare:89 | ||||
chr5:142326040-142326166 | Common:1; Rare:31 | ||||
chr5:143404442-143404617 | Common:2; Rare:36 | ||||
chr5:144170551-144170749 | Common:1; Rare:76 | ||||
chr5:146182501-146182841 | Common:3; Rare:91 | ||||
chr5:148383828-148384021 | Rare:56 | ||||
chr5:149141392-149141591 | Rare:52 |