Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:75052502-75052718 | Common:2; Rare:48 | ||||
chr5:80070129-80070319 | Common:1; Rare:35 | ||||
chr5:80072143-80072379 | Common:2; Rare:63 | ||||
chr5:80442262-80442448 | Rare:30 | ||||
chr5:87369614-87369847 | Rare:33; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr5:93621490-93621717 | Common:2; Rare:55 | ||||
chr5:108728265-108728418 | Rare:52 | ||||
chr5:112160827-112160920 | Common:2; Rare:51 | ||||
chr5:123025954-123026243 | Common:2; Rare:48 | ||||
chr5:128082014-128082078 | Common:1; Rare:14 | ||||
chr5:128083024-128083173 | Common:8; Rare:49 | ||||
chr5:132259276-132259353 | Rare:20 | ||||
chr5:132264079-132264265 | Common:1; Rare:34 | ||||
chr5:132265695-132265810 | Rare:15 | ||||
chr5:132293561-132293771 | Common:2; Rare:55 |