ID: 127897945 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:96894224-96894852 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (97639225..97639853) | | |
ID: 127897944 | NANOG hESC enhancer GRCh37_chrX:96852041-96852542 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (97597042..97597543) | | |
ID: 127897943 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:96838907-96839554 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (97583908..97584555) | | |
ID: 127897942 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:96838258-96838906 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (97583259..97583907) | | |
ID: 127897941 | OCT4-NANOG hESC enhancer GRCh37_chrX:96759203-96760072 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (97504204..97505073) | | |
ID: 127897940 | OCT4-NANOG hESC enhancer GRCh37_chrX:96737386-96738055 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (97482387..97483056) | | |
ID: 127897939 | NANOG hESC enhancer GRCh37_chrX:96596543-96597044 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (97341544..97342045) | | |
ID: 127897938 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:96544890-96545450 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (97289891..97290451) | | |
ID: 127897937 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:96544328-96544889 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (97289329..97289890) | | |
ID: 127897936 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chrX:96506917-96507740 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (97251918..97252741) | | |
ID: 127897935 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:96455541-96456245 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (97200542..97201246) | | |
ID: 127897934 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:96454836-96455540 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (97199837..97200541) | | |
ID: 127897933 | OCT4-NANOG hESC enhancer GRCh37_chrX:96282448-96283050 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (97027449..97028051) | | |
ID: 127897932 | H3K27ac hESC enhancer GRCh37_chrX:96070683-96071183 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (96815684..96816184) | | |
ID: 127897931 | H3K27ac hESC enhancer GRCh37_chrX:96070182-96070682 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (96815183..96815683) | | |
ID: 127897930 | NANOG-H3K27ac hESC enhancer GRCh37_chrX:95985965-95986513 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (96730966..96731514) | | |
ID: 127897929 | H3K27ac hESC enhancer GRCh37_chrX:95940345-95941058 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (96685346..96686059) | | |
ID: 127897928 | H3K27ac hESC enhancer GRCh37_chrX:95939629-95940344 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (96684630..96685345) | | |
ID: 126863292 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chrX:96871608-96872807 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (97616609..97617808) | | |
ID: 126863291 | MED14-independent group 3 enhancer GRCh37_chrX:96374110-96375309 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (97119111..97120310) | | |