ID: 127894658 | H3K4me1 hESC enhancer GRCh37_chr21:39201385-39202107 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37829083..37829805) | | |
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: 126653363 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr21:39345582-39346781 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37973279..37974478) | | |
ID: 110121448 | VISTA enhancer hs1811 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37855304..37856921) | | |
ID: 105372799 | KCNJ6 antisense RNA 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37518636..37740702) | KCNJ6-IT1 | |
ID: 101928368 | uncharacterized LOC101928368 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37751537..37760512) | | |
ID: 10281 | Down syndrome critical region 4 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (38054011..38121360, complement) | DCRB, DSCRB | 604829 |
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 |