ID: 127888713 | NANOG hESC enhancer GRCh37_chr18:6782830-6783412 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (6782831..6783413) | | |
ID: 127888712 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr18:6752537-6753112 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (6752538..6753113) | | |
ID: 127888711 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr18:6751961-6752536 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (6751962..6752537) | | |
ID: 127888710 | H3K27ac hESC enhancer GRCh37_chr18:6740951-6741451 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (6740952..6741452) | | |
ID: 127888709 | H3K27ac hESC enhancer GRCh37_chr18:6740450-6740950 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (6740451..6740951) | | |
ID: 127888708 | H3K27ac hESC enhancer GRCh37_chr18:6729485-6730448 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (6729486..6730449) | | |
ID: 127888707 | NANOG-H3K4me1 hESC enhancer GRCh37_chr18:6605546-6606358 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (6605547..6606359) | | |
ID: 107985176 | uncharacterized LOC107985176 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (6568979..6647163, complement) | | |
ID: 106481468 | RNA, U6 small nuclear 916, pseudogene [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (6936912..6937020, complement) | | |
ID: 106480374 | RNA, 7SL, cytoplasmic 282, pseudogene [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (6601540..6601836) | | |
ID: 101927168 | ARHGAP28 antisense RNA 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (6728927..6729862, complement) | | |
ID: 100421167 | SCML2 pseudogene 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (6926974..6928215) | | |
ID: 400643 | long intergenic non-protein coding RNA 668 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (6925474..6929869, complement) | | |
ID: 79822 | Rho GTPase activating protein 28 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (6729716..6915716) | | 610592 |