ID: 127894517 | NANOG-H3K27ac hESC enhancer GRCh37_chr21:32955714-32956498 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (31583401..31584185) | | |
ID: 127894516 | H3K27ac hESC enhancer GRCh37_chr21:32931173-32931985 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (31558860..31559672) | | |
ID: 127894515 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:32929546-32930359 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (31557233..31558046) | | |
ID: 127894514 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr21:32926455-32927174 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (31554142..31554861) | | |
ID: 127894513 | H3K27ac hESC enhancer GRCh37_chr21:32925735-32926454 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (31553422..31554141) | | |
ID: 127894512 | NANOG-H3K4me1 hESC enhancer GRCh37_chr21:32917456-32918188 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (31545143..31545875) | | |
ID: 127894511 | H3K4me1 hESC enhancer GRCh37_chr21:32894311-32894810 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (31521998..31522497) | | |
ID: 127894510 | H3K27ac hESC enhancer GRCh37_chr21:32868091-32868590 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (31495778..31496277) | | |
ID: 127894509 | H3K27ac hESC enhancer GRCh37_chr21:32867589-32868090 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (31495276..31495777) | | |
ID: 127894508 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:32842913-32843876 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (31470600..31471563) | | |
ID: 127894507 | H3K4me1 hESC enhancer GRCh37_chr21:32554821-32555320 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (31182504..31183003) | | |
ID: 127894506 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr21:32530991-32531520 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (31158674..31159203) | | |
ID: 126653341 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr21:32738744-32739943 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (31366429..31367628) | | |
ID: 126653340 | MED14-independent group 3 enhancer GRCh37_chr21:32710674-32711873 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (31338359..31339558) | | |
ID: 125418059 | Sharpr-MPRA regulatory region 15669 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (31176032..31176326) | | |
ID: 124908125 | uncharacterized LOC124908125 [Homo sapiens (human)] | | | |
ID: 105372777 | uncharacterized LOC105372777 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (31255420..31262458) | | |
ID: 100129168 | MTRES1 pseudogene 2 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (31452452..31453316) | | |
ID: 728299 | keratin associated protein 19-8 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (31038159..31038476, complement) | | |
ID: 150051 | TIAM1 antisense RNA 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (31559233..31560487) | | |