ID: 127882635 | H3K4me1 hESC enhancer GRCh37_chr16:576271-576832 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (526271..526832) | | |
ID: 127882631 | H3K4me1 hESC enhancer GRCh37_chr16:537093-537971 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (487093..487971) | | |
ID: 127882630 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:535039-535544 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (485039..485544) | | |
ID: 127882629 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:534533-535038 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (484533..485038) | | |
ID: 127882628 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:532003-532508 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (482003..482508) | | |
ID: 127882627 | H3K4me1 hESC enhancer GRCh37_chr16:516870-517498 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (466870..467498) | | |
ID: 127882626 | H3K4me1 hESC enhancer GRCh37_chr16:516240-516869 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (466240..466869) | | |
ID: 127882625 | H3K4me1 hESC enhancer GRCh37_chr16:495823-496323 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (445823..446323) | | |
ID: 127882624 | H3K4me1 hESC enhancer GRCh37_chr16:495322-495822 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (445322..445822) | | |
ID: 127882623 | H3K4me1 hESC enhancer GRCh37_chr16:492123-492661 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (442123..442661) | | |
ID: 107987417 | uncharacterized LOC107987417 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (491373..493540, complement) | | |
ID: 64493 | long intergenic non-protein coding RNA 235 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (526847..527407, complement) | C16orf10, LA16c-356B8.1, NCRNA00235 | |
ID: 26063 | 2,4-dienoyl-CoA reductase 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (401885..412482) | PDCR, SDR17C1 | 615839 |
ID: 9727 | RAB11 family interacting protein 3 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (425649..523011) | CART1, FIP3, FIP3-Rab11, Rab11-FIP3 | 608738 |
ID: 6650 | calpain 15 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (527712..554636) | OGIN, SOLH | 603267 |