| ID: 129664260 | ReSE screen-validated silencer GRCh37_chr18:47057605-47057776 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (49531235..49531406) | | |
| ID: 129390994 | MPRA-validated peak3145 silencer [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (49638516..49638716) | | |
| ID: 127889305 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr18:47139848-47140723 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (49613478..49614353) | | |
| ID: 127889304 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr18:47138971-47139847 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (49612601..49613477) | | |
| ID: 127889303 | H3K4me1 hESC enhancer GRCh37_chr18:47088634-47089134 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (49562264..49562764) | | |
| ID: 127889302 | OCT4-NANOG hESC enhancer GRCh37_chr18:47042044-47042658 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (49515674..49516288) | | |
| ID: 127889301 | NANOG-H3K27ac hESC enhancer GRCh37_chr18:47026295-47027190 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (49499925..49500820) | | |
| ID: 127889300 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr18:47018229-47018849 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (49491859..49492479) | | |
| ID: 126862743 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr18:47135425-47136624 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (49609055..49610254) | | |
| ID: 126862742 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr18:47076971-47078170 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (49550601..49551800) | | |
| ID: 112268210 | uncharacterized LOC112268210 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (49650514..49653475) | | |
| ID: 105372112 | uncharacterized LOC105372112 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (49612692..49740483) | | |
| ID: 101928144 | long intergenic non-protein coding RNA 2837 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (49499377..49527526) | | |
| ID: 100526842 | RPL17-C18orf32 readthrough [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (49481178..49492465, complement) | PD-1, RPL17 | |
| ID: 100420752 | signal recognition particle 72 pseudogene 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (49495040..49496897, complement) | | |
| ID: 100129143 | single-strand-selective monofunctional uracil-DNA glycosylase 1 pseudogene 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (49650350..49651162) | | |
| ID: 26790 | small nucleolar RNA, C/D box 58B [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (49491664..49491729, complement) | RNU58B, U58b | |
| ID: 9388 | lipase G, endothelial type [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (49561479..49599185) | EDL, EL, PRO719 | 603684 |
| ID: 6139 | ribosomal protein L17 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (49488481..49492465, complement) | L17, PD-1, RPL23, uL22 | 603661 |