ID: 129664926 | ReSE screen-validated silencer GRCh37_chrX:35063242-35063449 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (35045125..35045332) | | |
ID: 127897400 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:34782794-34783536 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (34764677..34765419) | | |
ID: 127897399 | NANOG hESC enhancer GRCh37_chrX:34611791-34612292 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (34593674..34594175) | | |
ID: 127897398 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:34578429-34578954 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (34560312..34560837) | | |
ID: 127897397 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:34577903-34578428 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (34559786..34560311) | | |
ID: 127897396 | NANOG-H3K27ac hESC enhancer GRCh37_chrX:34577375-34577902 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (34559258..34559785) | | |
ID: 127897395 | OCT4-NANOG hESC enhancer GRCh37_chrX:34575763-34576344 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (34557646..34558227) | | |
ID: 127897394 | H3K4me1 hESC enhancer GRCh37_chrX:34499547-34500046 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (34481430..34481929) | | |
ID: 107985674 | uncharacterized LOC107985674 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (34337693..34345729) | | |
ID: 392440 | MAGE family member B18 pseudogene [Homo sapiens (human)] | Chromosome X, NC_000023.11 (35058966..35059973) | | |
ID: 392439 | SRSF2 pseudogene 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (34387722..34388437) | | |
ID: 170062 | family with sequence similarity 47 member B [Homo sapiens (human)] | Chromosome X, NC_000023.11 (34942796..34944915) | | |
ID: 83604 | transmembrane protein 47 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (34627075..34657285, complement) | BCMP1, TM4SF10, VAB-9 | 300698 |