| ID: 130009995 | ATAC-STARR-seq lymphoblastoid silent region 5456 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (98142835..98143144) | | |
| ID: 130009994 | ATAC-STARR-seq lymphoblastoid silent region 5455 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (98142545..98142594) | | |
| ID: 127826696 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:98716739-98717336 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (98064485..98065082) | | |
| ID: 127826695 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:98716143-98716738 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (98063889..98064484) | | |
| ID: 127826694 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:98713754-98714350 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (98061500..98062096) | | |
| ID: 124909514 | Sharpr-MPRA regulatory region 2492 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (98173515..98173809) | | |
| ID: 121468003 | Sharpr-MPRA regulatory region 10209 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (98202095..98202389) | | |
| ID: 107984566 | uncharacterized LOC107984566 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (98073195..98075473) | | |
| ID: 105370328 | uncharacterized LOC105370328 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (98066312..98143910, complement) | | |
| ID: 100873852 | RN7SK pseudogene 8 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (98203835..98204192, complement) | | |
| ID: 100462790 | ferritin light chain pseudogene 8 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (97986949..97987225, complement) | | |
| ID: 100422881 | microRNA 3170 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (98208524..98208600) | mir-3170 | |
| ID: 140432 | ring finger protein 113B [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (98175785..98177269, complement) | RNF161, ZNF183L1, bA10G5.1 | |
| ID: 10160 | FERM, ARH/RhoGEF and pleckstrin domain protein 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (98142589..98455176) | CDEP-IT1, GLCC1, PLEKHC2, PPP1R75, FARP1 | 602654 |
| ID: 3843 | importin 5 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (97953675..98024296) | IMB3, KPNB3, Pse1, RANBP5, imp5 | 602008 |