Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:119355819-119356021 | Common:2; Rare:51 | ||||
chr5:122845295-122845621 | Common:3; Rare:109 | ||||
chr5:123036657-123036973 | Common:2; Rare:79 | ||||
chr5:126595176-126595337 | Common:3; Rare:77; Clinvar:5; Clinvar (benign):8 | ||||
chr5:127030501-127030776 | Common:2; Rare:67 | ||||
chr5:131263911-131264099 | Rare:68 | ||||
chr5:131635159-131635326 | Common:1; Rare:72 | ||||
chr5:131796978-131797202 | Rare:62 | ||||
chr5:132369583-132369760 | Common:3; Rare:53 | ||||
chr5:132410603-132410946 | Common:1; Rare:67 | ||||
chr5:132866457-132866687 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
chr5:133051880-133052348 | Common:1; Rare:146 | ||||
chr5:133968580-133968722 | Rare:53 | ||||
chr5:134004647-134004838 | Common:1; Rare:72 | ||||
chr5:134004923-134005198 | Rare:65 |