| ID: 130009569 | ATAC-STARR-seq lymphoblastoid silent region 5263 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36346243..36346292) | | |
| ID: 129390600 | MPRA-validated peak2068 silencer [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36211318..36211518) | | |
| 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: 127826102 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:36728605-36729169 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36154468..36155032) | | |
| ID: 124855084 | Sharpr-MPRA regulatory region 14903 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36276492..36276786) | | |
| ID: 112163654 | Sharpr-MPRA regulatory region 3304 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36324272..36324566) | | |
| ID: 107984604 | uncharacterized LOC107984604 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36156913..36163886, complement) | | |
| ID: 100873774 | RNA, U6 small nuclear 71, pseudogene [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36267168..36267274) | RNU6-71 | |
| ID: 100526761 | CCDC169-SOHLH2 readthrough [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36168217..36297814, complement) | C13orf38-SOHLH2, SOHLH2, TEB1 | |
| ID: 100507135 | SPART antisense RNA 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36346431..36369735) | C13orf43, SPG20-AS1, SPG20OS | |
| ID: 100189524 | nuclear-encoded mitochondrial tRNA-Gln (TTG) 10-1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36065610..36065681, complement) | TRNAQ50P | |
| ID: 728591 | coiled-coil domain containing 169 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36222004..36297814, complement) | C13orf38 | |
| ID: 54937 | spermatogenesis and oogenesis specific basic helix-loop-helix 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (36168217..36214556, complement) | SOSF2, SPATA28, TEB1, bHLHe81 | 616066 |