| ID: 127886697 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:36904187-36904722 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38747934..38748469) | | |
| ID: 127886696 | H3K4me1 hESC enhancer GRCh37_chr17:36902394-36903158 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38746141..38746905) | | |
| ID: 127886695 | H3K4me1 hESC enhancer GRCh37_chr17:36901628-36902393 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38745375..38746140) | | |
| ID: 127886694 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:36898365-36899265 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38742112..38743012) | | |
| ID: 127886693 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:36891176-36891703 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38734923..38735450) | | |
| ID: 127886692 | H3K4me1 hESC enhancer GRCh37_chr17:36887390-36887927 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38731137..38731674) | | |
| ID: 127886691 | H3K4me1 hESC enhancer GRCh37_chr17:36881911-36882602 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38725658..38726349) | | |
| ID: 108004529 | control region 19 heart enhancer [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38728738..38728960) | | |
| ID: 105371762 | uncharacterized LOC105371762 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38719088..38720319, complement) | | |
| ID: 100873688 | RNA, 5S ribosomal pseudogene 440 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38731802..38731920, complement) | RN5S440 | |
| ID: 100616153 | microRNA 4726 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38719691..38719748) | | |
| ID: 100287808 | uncharacterized LOC100287808 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38749034..38751752) | | |
| ID: 100189176 | tRNA-Asn (anticodon GTT) 2-5 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38751781..38751854, complement) | TRNAN17 | |
| ID: 284106 | CDGSH iron sulfur domain 3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38730341..38735605) | MiNT, Miner2 | 611933 |
| ID: 7703 | polycomb group ring finger 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38733898..38749792, complement) | MEL-18, RNF110, TPFS, ZNF144 | 600346 |
| ID: 4302 | MLLT6, PHD finger containing [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38705273..38729795) | AF17 | 600328 |