ID: 129664742 | ReSE screen-validated silencer GRCh37_chr21:44908716-44908853 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43488836..43488973) | | |
ID: 129664741 | ReSE screen-validated silencer GRCh37_chr21:44876822-44877032 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43456942..43457152) | | |
ID: 128316804 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:44931227-44931922 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43511347..43512042) | | |
ID: 128316803 | H3K4me1 hESC enhancer GRCh37_chr21:44928045-44928546 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43508165..43508666) | | |
ID: 128316802 | H3K4me1 hESC enhancer GRCh37_chr21:44924427-44925037 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43504547..43505157) | | |
ID: 128316801 | H3K4me1 hESC enhancer GRCh37_chr21:44923814-44924426 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43503934..43504546) | | |
ID: 128316800 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:44922889-44923698 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43503009..43503818) | | |
ID: 128316799 | H3K4me1 hESC enhancer GRCh37_chr21:44918667-44919571 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43498787..43499691) | | |
ID: 128316798 | H3K4me1 hESC enhancer GRCh37_chr21:44912277-44913132 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43492397..43493252) | | |
ID: 128316797 | H3K4me1 hESC enhancer GRCh37_chr21:44905292-44906122 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43485412..43486242) | | |
ID: 128316796 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:44882521-44883518 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43462641..43463638) | | |
ID: 128316795 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:44875523-44876522 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43455643..43456642) | | |
ID: 128316794 | H3K4me1 hESC enhancer GRCh37_chr21:44874448-44875423 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43454568..43455543) | | |
ID: 128316793 | H3K27ac hESC enhancer GRCh37_chr21:44867273-44867892 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43447393..43448012) | | |
ID: 128316792 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:44866033-44866652 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43446153..43446772) | | |
ID: 128316791 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:44865413-44866032 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43445533..43446152) | | |
ID: 128316790 | H3K4me1 hESC enhancer GRCh37_chr21:44854193-44854692 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43434313..43434812) | | |
ID: 128316789 | H3K4me1 hESC enhancer GRCh37_chr21:44853691-44854192 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43433811..43434312) | | |
ID: 128316788 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:44834223-44834804 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43414343..43414924) | | |
ID: 125418081 | Sharpr-MPRA regulatory region 10850 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43430729..43431023) | | |