| ID: 127826147 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:41019797-41020402 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (40445551..40446265) | | |
| ID: 127826146 | H3K4me1 hESC enhancer GRCh37_chr13:40956871-40957426 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (40382734..40383289) | | |
| ID: 127826145 | H3K4me1 hESC enhancer GRCh37_chr13:40926515-40927014 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (40352378..40352877) | | |
| ID: 126861747 | BRD4-independent group 4 enhancer GRCh37_chr13:41092118-41093317 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (40517981..40519180) | | |
| ID: 124855091 | Sharpr-MPRA regulatory region 6999 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (40537572..40537866) | | |
| ID: 124855090 | Sharpr-MPRA regulatory region 8959 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (40317752..40318046) | | |
| ID: 108318668 | LINC00598 intron ENCODE-defined enhancer [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (40406361..40407004) | | |
| ID: 100873846 | RN7SK pseudogene 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (40407122..40407440, complement) | | |
| ID: 100862672 | RNY3 pseudogene 9 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (40226827..40226932) | | |
| ID: 646982 | long intergenic non-protein coding RNA 598 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (40347132..40481004, complement) | lncFOXO1 | 619008 |