Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:131170686-131171002 | Common:1; Rare:67; Clinvar (benign):1 | ||||
chr5:131635160-131635439 | Common:1; Rare:106 | ||||
chr5:131796943-131797213 | Rare:77 | ||||
chr5:132257476-132257732 | Common:8; Rare:67 | ||||
chr5:132410603-132410951 | Common:1; Rare:67 | ||||
chr5:132490770-132491020 | Rare:64 | ||||
chr5:132556858-132557020 | Rare:60; Clinvar:1 | ||||
chr5:132866435-132866688 | Common:1; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
chr5:132963625-132963842 | Common:1; Rare:49 | ||||
chr5:133051640-133052354 | Common:3; Rare:231 | ||||
chr5:133968554-133968737 | Rare:73 | ||||
chr5:134004504-134004861 | Common:2; Rare:123 | ||||
chr5:134004867-134005010 | Rare:36 | ||||
chr5:134226039-134226417 | Common:1; Rare:119 | ||||
chr5:134371027-134371588 | Common:5; Rare:182 |