| ID: 129994139 | ATAC-STARR-seq lymphoblastoid silent region 16139 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (80481458..80481567) | | |
| ID: 127403253 | H3K27ac hESC enhancer GRCh37_chr5:79793017-79793517 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (80497198..80497698) | | |
| ID: 127403252 | OCT4-NANOG hESC enhancer GRCh37_chr5:79789343-79789929 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (80493524..80494110) | | |
| ID: 127403251 | H3K27ac hESC enhancer GRCh37_chr5:79783523-79784024 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (80487704..80488205) | | |
| ID: 127403250 | H3K27ac hESC enhancer GRCh37_chr5:79703845-79704643 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (80408026..80408824) | | |
| ID: 123497922 | H3K27ac hESC enhancer GRCh37_chr5:79784025-79784524 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (80488206..80488705) | | |
| ID: 121232370 | FAM151B divergent transcript [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (80482800..80487946, complement) | | |
| ID: 106479660 | RNA, U6 small nuclear 211, pseudogene [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (80365727..80365832, complement) | | |
| ID: 100271376 | RPS27A pseudogene 9 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (80498493..80499028, complement) | RPS27A_3_585 | |
| ID: 100127893 | ribosomal protein L7 pseudogene 24 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (80500312..80501468) | RPL7_8_586 | |
| ID: 644037 | heterogeneous nuclear ribonucleoprotein A1 pseudogene 12 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (80358880..80360099, complement) | | |
| ID: 167555 | family with sequence similarity 151 member B [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (80488100..80542563) | UNQ9217 | |
| ID: 9765 | zinc finger FYVE-type containing 16 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (80407610..80483379) | PPP1R69 | 608880 |