ID: 127897369 | NANOG hESC enhancer GRCh37_chrX:30259792-30260365 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30241675..30242248) | | |
ID: 127897368 | NANOG hESC enhancer GRCh37_chrX:30246492-30247101 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30228375..30228984) | | |
ID: 127897367 | OCT4-NANOG hESC enhancer GRCh37_chrX:30237442-30238027 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30219325..30219910) | | |
ID: 127897366 | H3K4me1 hESC enhancer GRCh37_chrX:30236871-30237370 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30218754..30219253) | | |
ID: 126863236 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chrX:30232864-30234063 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30214747..30215946) | | |
ID: 107985632 | uncharacterized LOC107985632 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30213333..30215520, complement) | | |
ID: 100420324 | MAGE family member A10 pseudogene [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30209387..30210238) | | |
ID: 4115 | MAGE family member B4 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30242000..30244187) | CT3.6 | 300153 |
ID: 4114 | MAGE family member B3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30230657..30237495) | CT3.5 | 300152 |
ID: 4113 | MAGE family member B2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30215563..30220089) | CT3.2, DAM6, MAGE-XP-2 | 300098 |
ID: 4112 | MAGE family member B1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (30243731..30252040) | CT3.1, DAM10, MAGE-Xp, MAGEL1 | 300097 |