ID: 126863334 | MED14-independent group 3 enhancer GRCh37_chrX:140991796-140992995 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (141904010..141905209) | | |
ID: 126863333 | MED14-independent group 3 enhancer GRCh37_chrX:140802566-140803765 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (141714410..141715609) | | |
ID: 728712 | SPANX family member A2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (141589708..141590762) | CT11.1, CT11.3, SPANX, SPANX-A, SPANX-C, SPANXA, SPANXC | 300493 |
ID: 645188 | uncharacterized LOC645188 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (141625866..141626744) | SPANX-L | |
ID: 619455 | SPANXA2 overlapping transcript 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (141502849..141649939) | CXorf18 | |
ID: 139081 | MAGE family member C3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (141838316..141897832) | CT7.2, HCA2, MAGE-C3, MAGEC4 | 300469 |
ID: 64648 | SPANX family member D [Homo sapiens (human)] | Chromosome X, NC_000023.11 (141697411..141698739, complement) | CT11.3, CT11.4, SPANX-C, SPANX-D, SPANX-E, SPANXC, SPANXE, dJ171K16.1 | 300670 |
ID: 9947 | MAGE family member C1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (141903894..141909374) | CT7, CT7.1 | 300223 |