Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:127030507-127030764 | Common:2; Rare:61 | ||||
chr5:131165194-131165401 | Common:2; Rare:87; Clinvar (benign):1 | ||||
chr5:131635184-131635398 | Common:1; Rare:83 | ||||
chr5:131796948-131797203 | Rare:74 | ||||
chr5:132294119-132294417 | Common:1; Rare:72 | ||||
chr5:132410769-132411017 | Rare:53 | ||||
chr5:132490754-132490978 | Rare:50 | ||||
chr5:132830612-132830776 | Rare:46 | ||||
chr5:132866564-132866694 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
chr5:133051851-133052357 | Common:1; Rare:162 | ||||
chr5:133968552-133968737 | Rare:74 | ||||
chr5:134004504-134004877 | Common:2; Rare:128 | ||||
chr5:134004883-134005085 | Rare:45 | ||||
chr5:134225537-134225622 | Common:1; Rare:30 | ||||
chr5:134226025-134226417 | Common:1; Rare:125 |