| ID: 127824656 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:82752536-82753096 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (82358757..82359317) | | |
| ID: 127824655 | H3K27ac hESC enhancer GRCh37_chr12:82751975-82752535 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (82358196..82358826) | | |
| ID: 127824654 | H3K4me1 hESC enhancer GRCh37_chr12:82707907-82708408 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (82314128..82314629) | | |
| ID: 127824653 | H3K27ac hESC enhancer GRCh37_chr12:82540979-82541568 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (82147200..82147789) | | |
| ID: 127824652 | H3K27ac hESC enhancer GRCh37_chr12:82514940-82515440 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (82121161..82121661) | | |
| ID: 127824651 | H3K4me1 hESC enhancer GRCh37_chr12:82151989-82152927 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (81758210..81759148) | | |
| ID: 127824650 | NANOG hESC enhancer GRCh37_chr12:82087706-82088318 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (81693927..81694539) | | |
| ID: 127824649 | H3K4me1 hESC enhancer GRCh37_chr12:82005227-82005726 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (81611448..81611947) | | |
| ID: 126861584 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr12:82495963-82497162 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (82102184..82103383) | | |
| ID: 105369873 | uncharacterized LOC105369873 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (82134895..82308315, complement) | | |
| ID: 105369872 | uncharacterized LOC105369872 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (81344078..81353236) | | |
| ID: 101928449 | long intergenic non-protein coding RNA 2426 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (81953719..81993133) | | |
| ID: 100312809 | vomeronasal 1 receptor 57 pseudogene [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (81868368..81869098) | | |
| ID: 84190 | methyltransferase like 25 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (82358529..82479239) | C12orf26 | |
| ID: 29080 | coiled-coil domain containing 59 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (82352303..82358805, complement) | BR22, HSPC128, TAP26 | 619280 |
| ID: 8499 | PTPRF interacting protein alpha 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (81257975..81759350, complement) | | 603143 |