Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:100052112-100052274 | Common:3; Rare:29 | ||||
chr5:108728251-108728488 | Rare:81 | ||||
chr5:112160555-112160911 | Common:4; Rare:111 | ||||
chr5:128082982-128083186 | Common:8; Rare:63 | ||||
chr5:132587644-132587950 | Common:1; Rare:62; Clinvar:8; Clinvar (benign):3 | ||||
chr5:134924045-134924128 | Rare:26 | ||||
chr5:134925377-134925434 | Rare:14 | ||||
chr5:134927024-134927101 | Common:2; Rare:16 | ||||
chr5:134927697-134927985 | Common:4; Rare:56 | ||||
chr5:134928076-134928381 | Common:3; Rare:53 | ||||
chr5:135355130-135355176 | Rare:14 | ||||
chr5:137752727-137752844 | Rare:19 | ||||
chr5:137752992-137753034 | Rare:11 | ||||
chr5:140676798-140676997 | Common:1; Rare:61; Clinvar:3 | ||||
chr5:141318748-141319101 | Common:1; Rare:80 |