| ID: 127897189 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:10141885-10142861 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10173845..10174821) | | |
| ID: 127897188 | H3K4me1 hESC enhancer GRCh37_chrX:10078177-10078894 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10110137..10110968) | | |
| ID: 127897187 | H3K4me1 hESC enhancer GRCh37_chrX:10077459-10078176 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10109419..10110136) | | |
| ID: 127897186 | H3K4me1 hESC enhancer GRCh37_chrX:10050926-10051426 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10082886..10083386) | | |
| ID: 127897185 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:10018119-10018742 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10050079..10050702) | | |
| ID: 127897184 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:10015531-10016163 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10047491..10048123) | | |
| ID: 127897183 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:10014897-10015530 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10046857..10047490) | | |
| ID: 127897182 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:10009285-10009817 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10041245..10041777) | | |
| ID: 127897181 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:10008750-10009284 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10040710..10041244) | | |
| ID: 127897180 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:9982293-9983176 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10014253..10015136) | | |
| ID: 127897179 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:9981409-9982292 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10013369..10014252) | | |
| ID: 126863207 | BRD4-independent group 4 enhancer GRCh37_chrX:10416979-10418178 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10448939..10450138) | | |
| ID: 121627958 | Sharpr-MPRA regulatory region 7563 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10119429..10119723) | | |
| ID: 55841 | WWC family member 3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10015254..10144474) | BM042 | 301089 |
| ID: 4281 | midline 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10445310..10833683, complement) | BBBG1, FXY, GBBB, GBBB1, MIDIN, OGS1, OS, OSX, RNF59, TRIM18, XPRF, ZNFXY | 300552 |
| ID: 1183 | chloride voltage-gated channel 4 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (10156975..10237660) | CLC4, ClC-4, ClC-4A, MRX15, MRX49, MRXSRC | 302910 |