| ID: 127823461 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:6078733-6079346 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (5969567..5970180) | | |
| ID: 127823460 | H3K4me1 hESC enhancer GRCh37_chr12:6076959-6077460 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (5967793..5968294) | | |
| ID: 127823459 | H3K4me1 hESC enhancer GRCh37_chr12:6030281-6030782 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (5921115..5921616) | | |
| ID: 127823458 | H3K4me1 hESC enhancer GRCh37_chr12:6017201-6017701 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (5908035..5908535) | | |
| ID: 127823457 | NANOG hESC enhancer GRCh37_chr12:5927975-5928488 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (5818809..5819322) | | |
| ID: 127823456 | H3K27ac hESC enhancer GRCh37_chr12:5921895-5922394 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (5812729..5813228) | | |
| ID: 127823455 | OCT4 hESC enhancer GRCh37_chr12:5681388-5681889 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (5572222..5572723) | | |
| ID: 127823454 | H3K4me1 hESC enhancer GRCh37_chr12:5626075-5626631 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (5516909..5517465) | | |
| ID: 126861431 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr12:6040249-6041448 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (5931083..5932282) | | |
| ID: 126861430 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr12:5916007-5917206 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (5806841..5808040) | | |
| ID: 126861429 | BRD4-independent group 4 enhancer GRCh37_chr12:5629720-5630919 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (5520554..5521753) | | |
| ID: 124902865 | uncharacterized LOC124902865 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (5506566..5526731) | | |
| ID: 124625891 | NANOG-H3K4me1 hESC enhancer GRCh37_chr12:5936424-5937202 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (5827258..5828036) | | |
| ID: 107832854 | meiotic recombination hotspot 12D [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (5789977..5792123) | | |
| ID: 107436002 | meiotic recombination hotspot F [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (5638845..5641797) | | |
| ID: 105369621 | uncharacterized LOC105369621 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (5881890..5912310) | | |
| ID: 101901829 | dynein light chain roadblock-type 1 pseudogene [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (5583761..5584445) | | |
| ID: 57101 | anoctamin 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (5562655..5946232, complement) | C12orf3, TMEM16B | 610109 |
| ID: 7450 | von Willebrand factor [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (5948877..6124670, complement) | F8VWF, VWD | 613160 |