| ID: 127274392 | H3K27ac hESC enhancer GRCh37_chr2:110839142-110839642 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (110081565..110082065) | | |
| ID: 127274391 | H3K27ac hESC enhancer GRCh37_chr2:110821474-110821974 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (110063897..110064397) | | |
| ID: 127274390 | H3K27ac hESC enhancer GRCh37_chr2:110812353-110812891 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (110054776..110055314) | | |
| ID: 127274389 | H3K27ac hESC enhancer GRCh37_chr2:110811814-110812352 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (110054237..110054775) | | |
| ID: 127274388 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:110806307-110807152 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (110048730..110049575) | | |
| ID: 127274387 | H3K4me1 hESC enhancer GRCh37_chr2:110804612-110805458 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (110047035..110047881) | | |
| ID: 127274386 | H3K4me1 hESC enhancer GRCh37_chr2:110800236-110800801 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (110042659..110043224) | | |
| ID: 127274385 | H3K4me1 hESC enhancer GRCh37_chr2:110797660-110798382 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (110040083..110040805) | | |
| ID: 127274384 | H3K4me1 hESC enhancer GRCh37_chr2:110793081-110793918 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (110035504..110036341) | | |
| ID: 127274383 | H3K4me1 hESC enhancer GRCh37_chr2:110789400-110790048 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (110031823..110032471) | | |
| ID: 127274382 | H3K4me1 hESC enhancer GRCh37_chr2:110788743-110789242 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (110031166..110031665) | | |
| ID: 127274381 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:110785874-110786695 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (110028297..110029118) | | |
| ID: 124906058 | uncharacterized LOC124906058 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (110032761..110035200, complement) | | |
| ID: 105373986 | uncharacterized LOC105373986 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (110042855..110048565, complement) | | |
| ID: 105373985 | uncharacterized LOC105373985 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (110027481..110028641, complement) | | |
| ID: 105373549 | uncharacterized LOC105373549 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (110039635..110041438, complement) | | |
| ID: 105373548 | uncharacterized LOC105373548 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (110035839..110039614, complement) | | |
| ID: 100616123 | microRNA 4436b-1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (110086433..110086523, complement) | MIR4436B, hsa-mir-4436b-1 | |
| ID: 100422994 | microRNA 4267 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (110069961..110070042, complement) | | |
| ID: 7851 | mal, T cell differentiation protein like [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (110083870..110118139, complement) | BENE | 602022 |