Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:172850147-172850442 | Common:1; Rare:56 | ||||
chr5:177455484-177455609 | Common:1; Rare:26 | ||||
chr5:178209173-178209471 | Common:1; Rare:102 | ||||
chr5:178209979-178210272 | Common:1; Rare:113 | ||||
chr5:179833399-179833707 | Common:7; Rare:105; Clinvar:4; Clinvar (benign):5 | ||||
chr5:180831551-180831718 | Common:2; Rare:71 | ||||
chr5:181189695-181189843 | Rare:26 | ||||
chr5:181264316-181264532 | Common:4; Rare:35 | ||||
chr6:434825-434903 | Common:1; Rare:35 | ||||
chr6:711398-711519 | Rare:16 | ||||
chr6:2855209-2855352 | Common:1; Rare:27 | ||||
chr6:2880321-2880380 | Rare:8 | ||||
chr6:2989932-2989957 | Rare:5 | ||||
chr6:6407394-6407691 | Common:2; Rare:58 | ||||
chr6:6587188-6587350 | Common:2; Rare:32 |