Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:27100427-27100582 | Common:3; Rare:48; Clinvar:4; Clinvar (benign):2 | ||||
chr10:27154310-27154480 | Rare:45 | ||||
chr10:27155252-27155426 | Common:6; Rare:80; Clinvar:2; Clinvar (benign):6 | ||||
chr10:27240740-27240874 | Rare:36 | ||||
chr10:27242072-27242186 | Common:1; Rare:49 | ||||
chr10:28532458-28532890 | Common:5; Rare:161 | ||||
chr10:29481660-29481952 | Common:2; Rare:61 | ||||
chr10:29486454-29486654 | Rare:50 | ||||
chr10:29634903-29635071 | Rare:34 | ||||
chr10:29735768-29736025 | Common:3; Rare:52 | ||||
chr10:30059491-30059734 | Common:1; Rare:81 | ||||
chr10:30115485-30115536 | Rare:11 | ||||
chr10:30434520-30434657 | Common:1; Rare:42 | ||||
chr10:31031841-31032033 | Common:1; Rare:74 | ||||
chr10:31318225-31318533 | Common:5; Rare:69 |