| ID: 127826122 | OCT4-NANOG hESC enhancer GRCh37_chr13:38169125-38169774 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (37594988..37595637) | | |
| ID: 127826121 | H3K27ac hESC enhancer GRCh37_chr13:38120407-38120907 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (37546270..37546770) | | |
| ID: 127826120 | NANOG-H3K27ac hESC enhancer GRCh37_chr13:37854517-37855076 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (37280380..37280939) | | |
| ID: 127826119 | H3K27ac hESC enhancer GRCh37_chr13:37853957-37854516 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (37279820..37280379) | | |
| ID: 127826118 | NANOG hESC enhancer GRCh37_chr13:37846978-37847479 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (37272841..37273342) | | |
| ID: 127826117 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr13:37772677-37773347 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (37198540..37199210) | | |
| ID: 124903159 | uncharacterized LOC124903159 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (37362170..37490833) | | |
| ID: 124855085 | Sharpr-MPRA regulatory region 1712 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (37395612..37395906) | | |
| ID: 105377814 | uncharacterized LOC105377814 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (37233202..37238760) | | |
| ID: 103695431 | long intergenic non-protein coding RNA 1048 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (37481464..37484784, complement) | | |
| ID: 100873845 | RN7SK pseudogene 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (37166370..37166658, complement) | | |
| ID: 100271551 | ribosomal protein S12 pseudogene 24 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (37220858..37221252, complement) | RPS12_12_1308 | |
| ID: 400121 | long intergenic non-protein coding RNA 547 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (37534940..37551536) | | |
| ID: 10631 | periostin [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (37562585..37598768, complement) | OSF-2, OSF2, PDLPOSTN, PN | 608777 |