Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:192037-192214 | Common:1; Rare:65 | ||||
chr5:194441-194780 | Rare:85 | ||||
chr5:784688-784842 | Common:2; Rare:47 | ||||
chr5:1633910-1634056 | Common:2; Rare:49 | ||||
chr5:1883331-1883477 | Common:1; Rare:30 | ||||
chr5:8457562-8457742 | Common:2; Rare:61 | ||||
chr5:14712964-14713132 | Rare:57; Clinvar (benign):1 | ||||
chr5:38482160-38482308 | Rare:32 | ||||
chr5:43066910-43067066 | Rare:58 | ||||
chr5:43575653-43575881 | Common:1; Rare:42 | ||||
chr5:55422837-55422926 | Rare:24 | ||||
chr5:65925587-65925904 | Rare:128 | ||||
chr5:76819575-76819822 | Common:2; Rare:58 | ||||
chr5:79697383-79697465 | Rare:19 | ||||
chr5:79744320-79744510 | Common:1; Rare:35 |