| ID: 129664927 | ReSE screen-validated silencer GRCh37_chrX:36451102-36451307 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (36432989..36433194) | | |
| ID: 127897405 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:36489007-36489587 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (36470924..36471504) | | |
| ID: 127897404 | NANOG hESC enhancer GRCh37_chrX:36233110-36233611 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (36214993..36215494) | | |
| ID: 127897403 | OCT4-NANOG hESC enhancer GRCh37_chrX:36216564-36217118 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (36198447..36199001) | | |
| ID: 127897402 | NANOG-H3K4me1 hESC enhancer GRCh37_chrX:35841387-35842135 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (35823270..35824018) | | |
| ID: 126863237 | MED14-independent group 3 enhancer GRCh37_chrX:36449855-36451054 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (36431742..36432941) | | |
| ID: 115482714 | H2A.L variant histone 1Q [Homo sapiens (human)] | Chromosome X, NC_000023.11 (36719918..36720221) | H2A.L.1P, H2AL1Q | |
| ID: 106481908 | RNA, U6 small nuclear 641, pseudogene [Homo sapiens (human)] | Chromosome X, NC_000023.11 (36021940..36022045, complement) | | |
| ID: 105373155 | uncharacterized LOC105373155 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (36720381..36746129) | | |
| ID: 101928627 | uncharacterized LOC101928627 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (36365626..36440292, complement) | | |
| ID: 100128345 | NFYC pseudogene 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (35761304..35762778) | | |
| ID: 100128083 | ribosomal protein S15a pseudogene 40 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (36374755..36375213, complement) | RPS15A_26_1770 | |
| ID: 646577 | high mobility group box 1 pseudogene 16 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (36211004..36211932) | | |
| ID: 286464 | cilia and flagella associated protein 47 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (35919734..36385317) | CHDC2, CXorf22, CXorf30, CXorf59, SPGF52, SPGFX3 | 301057 |
| ID: 139604 | MAGE family member B16 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (35798342..35803772) | | 300762 |