Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:50093519-50093610 | Rare:14 | ||||
chr6:52420942-52421008 | Rare:14 | ||||
chr6:53793657-53793794 | Common:2; Rare:22 | ||||
chr6:57961347-57961658 | Common:2; Rare:97 | ||||
chr6:63346478-63346669 | Common:1; Rare:43 | ||||
chr6:71407394-71407729 | Common:1; Rare:65 | ||||
chr6:71414577-71414851 | Common:1; Rare:62 | ||||
chr6:71420797-71421018 | Common:2; Rare:74 | ||||
chr6:73517686-73518265 | Common:2; Rare:154 | ||||
chr6:75087728-75087941 | Common:1; Rare:30 | ||||
chr6:75113690-75113819 | Common:1; Rare:40; Clinvar (benign):1 | ||||
chr6:78947717-78948047 | Common:1; Rare:66 | ||||
chr6:78954894-78955032 | Common:2; Rare:38 | ||||
chr6:78966691-78966994 | Common:1; Rare:62 | ||||
chr6:78984772-78984829 | Rare:11 |