Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:122845345-122845621 | Common:3; Rare:92 | ||||
chr5:124748820-124748997 | Common:1; Rare:46 | ||||
chr5:126595192-126595337 | Common:3; Rare:67; Clinvar:1; Clinvar (benign):8 | ||||
chr5:127030549-127030764 | Common:2; Rare:49 | ||||
chr5:127073471-127073544 | Common:3; Rare:20 | ||||
chr5:127517484-127517696 | Common:7; Rare:94 | ||||
chr5:131165204-131165382 | Common:2; Rare:76; Clinvar (benign):1 | ||||
chr5:131170660-131171002 | Common:1; Rare:79; Clinvar (benign):1 | ||||
chr5:131635173-131635446 | Common:1; Rare:103 | ||||
chr5:131796970-131797221 | Rare:68 | ||||
chr5:132257476-132257727 | Common:8; Rare:65 | ||||
chr5:132410603-132410922 | Common:1; Rare:62 | ||||
chr5:132490774-132491020 | Rare:64 | ||||
chr5:132737506-132737579 | Rare:25 | ||||
chr5:132777233-132777360 | Rare:30 |