| ID: 132088598 | Neanderthal introgressed variant-containing enhancer experimental_1277 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (170287462..170287631) | | |
| ID: 129388629 | MPRA-validated peak452 silencer [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (170519115..170519315) | | |
| ID: 127270814 | H3K4me1 hESC enhancer GRCh37_chr1:170637613-170638135 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (170668472..170668994) | | |
| ID: 127270813 | H3K4me1 hESC enhancer GRCh37_chr1:170637090-170637612 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (170667949..170668471) | | |
| ID: 127270812 | H3K4me1 hESC enhancer GRCh37_chr1:170633905-170634765 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (170664764..170665624) | | |
| ID: 127270811 | NANOG hESC enhancer GRCh37_chr1:170632177-170632704 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (170663036..170663563) | | |
| ID: 127270810 | H3K4me1 hESC enhancer GRCh37_chr1:170600473-170600972 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (170631332..170631831) | | |
| ID: 127270809 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr1:170456497-170457212 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (170487356..170488071) | | |
| ID: 127270808 | NANOG hESC enhancer GRCh37_chr1:170284235-170284736 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (170315094..170315595) | | |
| ID: 126805914 | BRD4-independent group 4 enhancer GRCh37_chr1:170607884-170609083 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (170638743..170639942) | | |
| ID: 126805913 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr1:170588042-170589241 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (170618901..170620100) | | |
| ID: 124904453 | uncharacterized LOC124904453 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (170567518..170570630) | | |
| ID: 105371610 | uncharacterized LOC105371610 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (170640913..170660283) | | |
| ID: 101928650 | GORAB antisense RNA 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (170461317..170532609, complement) | | |
| ID: 100129402 | HAUS augmin like complex subunit 4 pseudogene 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (170368922..170370369, complement) | | |
| ID: 284688 | long intergenic non-protein coding RNA 1142 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (170271405..170284208, complement) | | |
| ID: 92344 | golgin, RAB6 interacting [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (170532166..170553834) | GO, NTKLBP1, SCYL1BP1 | 607983 |
| ID: 5396 | paired related homeobox 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (170662768..170739421) | AGOTC, PHOX1, PMX1, PRX-1, PRX1 | 167420 |