| ID: 127898315 | H3K4me1 hESC enhancer GRCh37_chrX:130960090-130960590 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (131826062..131826562) | | |
| ID: 127898314 | H3K4me1 hESC enhancer GRCh37_chrX:130937597-130938097 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (131803569..131804069) | | |
| ID: 127898313 | H3K4me1 hESC enhancer GRCh37_chrX:130937096-130937596 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (131803068..131803568) | | |
| ID: 127898312 | NANOG hESC enhancer GRCh37_chrX:130854476-130855009 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (131720448..131720981) | | |
| ID: 127898311 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:130851242-130851768 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (131717214..131717740) | | |
| ID: 127898310 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:130798263-130798901 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (131664250..131664888) | | |
| ID: 126863319 | MED14-independent group 3 enhancer GRCh37_chrX:131057048-131058247 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (131923020..131924219) | | |
| ID: 121627981 | Sharpr-MPRA regulatory region 13107 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (131816841..131817135) | | |
| ID: 121627980 | Sharpr-MPRA regulatory region 13451 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (131768241..131768535) | | |
| ID: 113875011 | Sharpr-MPRA regulatory region 4069 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (131793081..131793375) | | |
| ID: 113875010 | Sharpr-MPRA regulatory region 5272 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (131710961..131711255) | | |
| ID: 102388891 | MAPK regulated corepressor interacting protein 2 pseudogene 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (131795372..131796170, complement) | FAM195CP | |
| ID: 100873565 | RNA, 5S ribosomal pseudogene 514 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (131938846..131938956, complement) | RN5S514 | |
| ID: 100506715 | PNKD pseudogene 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (131803129..131803756, complement) | | |
| ID: 474167 | heparin binding growth factor pseudogene 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (131646640..131648237) | HDGFP | |
| ID: 286467 | firre intergenic repeating RNA element [Homo sapiens (human)] | Chromosome X, NC_000023.11 (131691525..131830643, complement) | LINC01200 | 300999 |