Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:23457555-23457808 | Common:4; Rare:86 | ||||
chr8:24955942-24956139 | Rare:77; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr8:24956608-24956742 | Common:2; Rare:31 | ||||
chr8:26382928-26383123 | Common:2; Rare:90 | ||||
chr8:26513855-26514025 | Rare:32 | ||||
chr8:27311188-27311478 | Common:7; Rare:121 | ||||
chr8:27772530-27772690 | Common:5; Rare:60 | ||||
chr8:27774238-27774592 | Common:3; Rare:77; Clinvar:3; Clinvar (benign):1 | ||||
chr8:28093054-28093206 | Common:1; Rare:50 | ||||
chr8:28490212-28490424 | Rare:39 | ||||
chr8:28494118-28494327 | Common:5; Rare:71 | ||||
chr8:28889905-28890430 | Rare:141 | ||||
chr8:29350653-29350925 | Common:2; Rare:66 | ||||
chr8:30083030-30083349 | Rare:109 | ||||
chr8:30156268-30156386 | Rare:28 |