| ID: 127826110 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr13:36896170-36896871 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36322033..36322734) | | |
| ID: 127826109 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr13:36895467-36896169 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36321330..36322032) | | |
| ID: 127826108 | H3K27ac hESC enhancer GRCh37_chr13:36894061-36894764 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36319924..36320627) | | |
| ID: 127826107 | H3K27ac hESC enhancer GRCh37_chr13:36891035-36891868 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36316898..36317731) | | |
| ID: 127826106 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr13:36890200-36891034 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36316063..36316897) | | |
| ID: 127826105 | NANOG hESC enhancer GRCh37_chr13:36887598-36888362 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36313461..36314225) | | |
| ID: 127826104 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr13:36872540-36873502 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36298403..36299365) | | |
| ID: 127826103 | H3K27ac hESC enhancer GRCh37_chr13:36871578-36872539 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36297441..36298402) | | |
| ID: 126861742 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr13:37011626-37012825 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36437489..36438688) | | |
| ID: 112163654 | Sharpr-MPRA regulatory region 3304 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36324272..36324566) | | |
| ID: 100526761 | CCDC169-SOHLH2 readthrough [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36168217..36297814, complement) | C13orf38-SOHLH2, SOHLH2, TEB1 | |
| ID: 100509927 | H2AC histone family pseudogene 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36490050..36490441, complement) | HIST1H2APS6 | |
| ID: 100507135 | SPART antisense RNA 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36346431..36369735) | C13orf43, SPG20-AS1, SPG20OS | |
| ID: 728591 | coiled-coil domain containing 169 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36222004..36297814, complement) | C13orf38 | |
| ID: 23111 | spartin [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36301638..36370180, complement) | SPG20, TAHCCP1 | 607111 |
| ID: 8900 | cyclin A1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36431517..36442870) | CT146 | 604036 |