ID: 127894657 | H3K4me1 hESC enhancer GRCh37_chr21:39200662-39201384 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37828360..37829082) | | |
ID: 127894656 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:39127657-39128504 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37755354..37756201) | | |
ID: 127894655 | H3K4me1 hESC enhancer GRCh37_chr21:39054697-39055209 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37682394..37682906) | | |
ID: 127894654 | H3K4me1 hESC enhancer GRCh37_chr21:39047357-39048256 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37675055..37675954) | | |
ID: 127894653 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:39040444-39041167 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37668142..37668865) | | |
ID: 127894652 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:39039721-39040443 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37667419..37668141) | | |
ID: 127894651 | H3K4me1 hESC enhancer GRCh37_chr21:39020347-39020847 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37648045..37648545) | | |
ID: 127894650 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:38965447-38966286 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37593145..37593984) | | |
ID: 127894649 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr21:38964609-38965446 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37592307..37593144) | | |
ID: 127894648 | NANOG-H3K27ac hESC enhancer GRCh37_chr21:38960011-38960798 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37587709..37588496) | | |
ID: 127894647 | H3K4me1 hESC enhancer GRCh37_chr21:38919349-38919849 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37547047..37547547) | | |
ID: 127894646 | H3K4me1 hESC enhancer GRCh37_chr21:38918848-38919348 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37546546..37547046) | | |
ID: 127894645 | NANOG-H3K27ac hESC enhancer GRCh37_chr21:38856065-38856652 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37483763..37484350) | | |
ID: 127894644 | H3K4me1 hESC enhancer GRCh37_chr21:38829655-38830166 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37457353..37457864) | | |
ID: 112694744 | Sharpr-MPRA regulatory region 302 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37563847..37564141) | | |
ID: 105372799 | KCNJ6 antisense RNA 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37518636..37740702) | KCNJ6-IT1 | |
ID: 105372798 | uncharacterized LOC105372798 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37560019..37570522) | | |
ID: 105372797 | uncharacterized LOC105372797 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37479033..37490045, complement) | | |
ID: 101928368 | uncharacterized LOC101928368 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37751537..37760512) | | |
ID: 3763 | potassium inwardly rectifying channel subfamily J member 6 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37607373..37916457, complement) | BIR1, GIRK-2, GIRK2, KATP-2, KATP2, KCNJ7, KIR3.2, KPLBS, hiGIRK2 | 600877 |