| ID: 127897142 | H3K4me1 hESC enhancer GRCh37_chrX:8696584-8697084 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (8728543..8729043) | | |
| ID: 127897141 | OCT4-NANOG hESC enhancer GRCh37_chrX:8689521-8690068 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (8721480..8722027) | | |
| ID: 127897140 | NANOG hESC enhancer GRCh37_chrX:8671941-8672658 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (8703900..8704617) | | |
| ID: 127897139 | H3K4me1 hESC enhancer GRCh37_chrX:8667852-8668352 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (8699811..8700311) | | |
| ID: 127897138 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:8657197-8658169 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (8689156..8690128) | | |
| ID: 127897137 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:8656224-8657196 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (8688183..8689155) | | |
| ID: 127897136 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:8618651-8619175 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (8650610..8651134) | | |
| ID: 127897135 | OCT4-NANOG hESC enhancer GRCh37_chrX:8611361-8612172 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (8643320..8644131) | | |
| ID: 127897134 | NANOG hESC enhancer GRCh37_chrX:8600996-8601504 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (8632955..8633463) | | |
| ID: 127897133 | NANOG hESC enhancer GRCh37_chrX:8476153-8476654 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (8508112..8508613) | | |
| ID: 126863201 | CDK7 strongly-dependent group 2 enhancer GRCh37_chrX:8725279-8726478 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (8757238..8758437) | | |
| ID: 126863200 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chrX:8462508-8463707 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (8494467..8495666) | | |
| ID: 125446267 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:8694042-8695034 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (8726001..8726993) | | |
| ID: 107985715 | long intergenic non-protein coding RNA 3113 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (8489674..8504564, complement) | | |
| ID: 100128801 | dorsal inhibitory axon guidance protein pseudogene 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (8783334..8784549, complement) | | |
| ID: 425054 | variable charge X-linked 3B [Homo sapiens (human)] | Chromosome X, NC_000023.11 (8464830..8466510) | VCX-C, VCXC | 300981 |
| ID: 171482 | family with sequence similarity 9 member A [Homo sapiens (human)] | Chromosome X, NC_000023.11 (8790795..8801383, complement) | TEX39A | 300477 |
| ID: 3730 | anosmin 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (8528874..8732137, complement) | ADMLX, HH1, HHA, KAL, KAL1, KALIG-1, KMS, WFDC19 | 300836 |