| ID: 127826313 | H3K4me1 hESC enhancer GRCh37_chr13:50952541-50953137 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50378405..50379001) | | |
| ID: 127826312 | OCT4-NANOG hESC enhancer GRCh37_chr13:50850586-50851108 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50276450..50276972) | | |
| ID: 127826311 | NANOG hESC enhancer GRCh37_chr13:50823191-50823706 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50249055..50249570) | | |
| ID: 127826310 | OCT4-NANOG hESC enhancer GRCh37_chr13:50715020-50715693 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50140884..50141557) | | |
| ID: 127826309 | H3K4me1 hESC enhancer GRCh37_chr13:50699798-50700508 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50125662..50126372) | | |
| ID: 127826308 | NANOG hESC enhancer GRCh37_chr13:50695956-50696481 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50121820..50122345) | | |
| ID: 127826307 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:50656434-50657229 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50082298..50083093) | | |
| ID: 126861776 | MED14-independent group 3 enhancer GRCh37_chr13:51102968-51104167 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50528832..50530349) | | |
| ID: 126861775 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr13:50818353-50819552 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50244217..50245416) | | |
| ID: 124900337 | uncharacterized LOC124900337 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50222838..50239344) | | |
| ID: 124900142 | Sharpr-MPRA regulatory region 6827 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50366833..50367127) | | |
| ID: 124900141 | Sharpr-MPRA regulatory region 84 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50081313..50081690) | | |
| ID: 121838575 | Sharpr-MPRA regulatory region 8262 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50636073..50636367) | | |
| ID: 103689915 | DLEU1 antisense RNA 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50520933..50527449, complement) | LINC01308 | |
| ID: 100271286 | ribosomal protein L18 pseudogene 10 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50099334..50099875) | RPL18_6_1311 | |
| ID: 100130718 | ribosomal protein L34 pseudogene 26 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50361378..50361811, complement) | RPL34_12_1312 | |
| ID: 406948 | microRNA 15a [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50049119..50049201, complement) | MIRN15A, hsa-mir-15a, miRNA15A, mir-15a | 609703 |
| ID: 145165 | ST13, Hsp70 interacting protein pseudogene 4 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50172018..50173616) | FAM10A4, FAM10A4P | |
| ID: 10301 | deleted in lymphocytic leukemia 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50082169..50528643) | BCMS, BCMS1, DLB1, DLEU2, LEU1, LEU2, LINC00021, NCRNA00021, XTP6 | 605765 |
| ID: 8847 | deleted in lymphocytic leukemia 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (49982549..50125541, complement) | ALT1, BCMSUN, DLB2, LEU2, LINC00022, MIR15AHG, NCRNA00022, RFP2, RFP2OS, TRIM13OS | 605766 |