ID: 127897707 | H3K4me1 hESC enhancer GRCh37_chrX:64722693-64723193 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65502813..65503313) | | |
ID: 127897706 | H3K4me1 hESC enhancer GRCh37_chrX:64722192-64722692 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65502312..65502812) | | |
ID: 127897705 | OCT4-NANOG hESC enhancer GRCh37_chrX:64713210-64713789 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65493330..65493909) | | |
ID: 127897704 | NANOG hESC enhancer GRCh37_chrX:64658617-64659137 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65438737..65439257) | | |
ID: 127897703 | NANOG hESC enhancer GRCh37_chrX:64612699-64613200 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65392819..65393320) | | |
ID: 127897702 | NANOG hESC enhancer GRCh37_chrX:64519957-64520668 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65300077..65300788) | | |
ID: 127897701 | H3K27ac hESC enhancer GRCh37_chrX:64416296-64416796 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65196416..65196916) | | |
ID: 127897700 | H3K27ac hESC enhancer GRCh37_chrX:64195850-64196393 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (64975970..64976513) | | |
ID: 125467757 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:64683306-64683834 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65463426..65463954) | | |
ID: 113875034 | Sharpr-MPRA regulatory region 9838 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65240989..65241283) | | |
ID: 105373239 | uncharacterized LOC105373239 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (64842760..64851049) | | |
ID: 100533843 | karyopherin subunit alpha 2 pseudogene [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65184951..65186216, complement) | | |
ID: 100131638 | chaperonin containing TCP1 subunit 4 pseudogene 2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65270912..65273021) | CCT4-1P | |
ID: 100129288 | mortality factor 4 like 1 pseudogene 5 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65327792..65331262, complement) | MORF4LP5 | |
ID: 650181 | PRXL2C pseudogene 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65356689..65357537, complement) | | |
ID: 645388 | AP1M2 pseudogene 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65469085..65470579) | | |
ID: 645381 | TLE family member 1 pseudogene 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65407877..65408674) | | |
ID: 340554 | zinc finger CCCH-type containing 12B [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65034826..65507887) | CXorf32, MCPIP2 | 300889 |
ID: 83957 | FERM domain containing 8 pseudogene 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65550622..65552421, complement) | | |
ID: 81887 | LAS1 like ribosome biogenesis factor [Homo sapiens (human)] | Chromosome X, NC_000023.11 (65512582..65534787, complement) | Las1, Las1-like, MRXSWTS, WTS, dJ475B7.2 | 300964 |