| ID: 127897260 | H3K4me1 hESC enhancer GRCh37_chrX:17674725-17675435 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (17656605..17657315) | | |
| ID: 127897259 | H3K4me1 hESC enhancer GRCh37_chrX:17674013-17674724 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (17655893..17656604) | | |
| ID: 127897258 | NANOG-H3K27ac hESC enhancer GRCh37_chrX:17653158-17653816 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (17635038..17635696) | | |
| ID: 127897257 | NANOG hESC enhancer GRCh37_chrX:17645772-17646631 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (17627652..17628511) | | |
| ID: 127897256 | NANOG-H3K4me1 hESC enhancer GRCh37_chrX:17567200-17567713 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (17549079..17549592) | | |
| ID: 127897255 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:17566170-17566684 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (17548049..17548563) | | |
| ID: 127897254 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:17565654-17566169 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (17547532..17548048) | | |
| ID: 127897253 | OCT4-NANOG hESC enhancer GRCh37_chrX:17427751-17428292 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (17409628..17410169) | | |
| ID: 127897252 | OCT4-NANOG hESC enhancer GRCh37_chrX:17403909-17404450 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (17385786..17386327) | | |
| ID: 126863217 | MED14-independent group 3 enhancer GRCh37_chrX:17767905-17769104 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (17749785..17750984) | | |
| ID: 124905270 | small nucleolar RNA U13 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (17357930..17358033) | | |
| ID: 117369447 | CHP1 pseudogene 3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (17705332..17705691, complement) | | |
| ID: 107985630 | family with sequence similarity 136 member G, pseudogene [Homo sapiens (human)] | Chromosome X, NC_000023.11 (17767702..17769423, complement) | | |
| ID: 105373142 | uncharacterized LOC105373142 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (17632258..17651754, complement) | | |
| ID: 101928389 | uncharacterized LOC101928389 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (17528435..17587160) | | |
| ID: 100873920 | NHS antisense RNA 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (17552349..17559127, complement) | | |
| ID: 100616249 | microRNA 4768 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (17425881..17425954) | | |
| ID: 100130461 | chromobox 1 pseudogene 4 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (17282351..17284552) | | |
| ID: 6322 | Scm polycomb group protein like 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (17737128..17754985) | | 300227 |
| ID: 4810 | NHS actin remodeling regulator [Homo sapiens (human)] | Chromosome X, NC_000023.11 (17375200..17735994) | CTRCT40, CXN, SCML1 | 300457 |