Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:127517470-127517712 | Common:7; Rare:106 | ||||
chr5:132866411-132866688 | Common:1; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
chr5:133051862-133052128 | Rare:97 | ||||
chr5:133968587-133968737 | Rare:53 | ||||
chr5:134004656-134004828 | Common:1; Rare:67 | ||||
chr5:134371395-134371574 | Common:3; Rare:70 | ||||
chr5:134632788-134632929 | Rare:28 | ||||
chr5:134648500-134648816 | Common:1; Rare:74 | ||||
chr5:134845824-134846057 | Rare:102 | ||||
chr5:138178943-138179172 | Common:3; Rare:50 | ||||
chr5:138753314-138753488 | Common:2; Rare:55 | ||||
chr5:140557448-140557515 | Rare:35 | ||||
chr5:140647594-140647876 | Common:5; Rare:115; Clinvar:4; Clinvar (benign):3 | ||||
chr5:140691353-140691515 | Common:1; Rare:52; Clinvar:5 | ||||
chr5:141636821-141636997 | Common:1; Rare:72 |