Variant report

Variant	rs10763312
Chromosome Location	chr10:57841516-57841517
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 118 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:108)

rs_ID	r²[population]
rs10450289	0.94[EUR][1000 genomes]
rs10763311	0.85[AFR][1000 genomes];0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10763313	0.95[EUR][1000 genomes]
rs10825743	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10825744	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10825746	0.95[EUR][1000 genomes]
rs10825747	0.95[EUR][1000 genomes]
rs10825748	0.95[EUR][1000 genomes]
rs10825749	0.95[EUR][1000 genomes]
rs10825750	0.95[EUR][1000 genomes]
rs11005209	0.94[EUR][1000 genomes]
rs12258449	0.95[EUR][1000 genomes]
rs1354038	0.94[EUR][1000 genomes]
rs1392724	0.95[EUR][1000 genomes]
rs1392725	0.94[EUR][1000 genomes]
rs1392726	0.95[EUR][1000 genomes]
rs1392727	0.94[EUR][1000 genomes]
rs1392730	0.94[EUR][1000 genomes]
rs1392731	0.94[EUR][1000 genomes]
rs1392732	0.94[EUR][1000 genomes]
rs1392733	0.94[EUR][1000 genomes]
rs1392734	0.94[EUR][1000 genomes]
rs1392735	0.94[EUR][1000 genomes]
rs1500737	0.94[EUR][1000 genomes]
rs1500761	0.96[EUR][1000 genomes]
rs1500762	0.96[EUR][1000 genomes]
rs1500769	0.91[EUR][1000 genomes]
rs1500770	0.94[EUR][1000 genomes]
rs1875290	0.96[EUR][1000 genomes]
rs1908352	0.96[EUR][1000 genomes]
rs1908353	0.96[EUR][1000 genomes]
rs1908354	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1908355	0.94[EUR][1000 genomes]
rs1908356	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1908357	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2069099	0.93[EUR][1000 genomes]
rs2088064	0.94[EUR][1000 genomes]
rs2088065	0.96[EUR][1000 genomes]
rs2201398	0.96[EUR][1000 genomes]
rs2201399	0.94[EUR][1000 genomes]
rs2893672	0.94[EUR][1000 genomes]
rs35407573	0.94[EUR][1000 genomes]
rs35626266	0.93[EUR][1000 genomes]
rs35835812	0.94[EUR][1000 genomes]
rs3913427	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4423113	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4935633	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4935634	0.81[EUR][1000 genomes]
rs4935636	0.81[EUR][1000 genomes]
rs60857714	0.94[EUR][1000 genomes]
rs61852256	0.94[EUR][1000 genomes]
rs7069579	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7072284	0.95[EUR][1000 genomes]
rs7073354	0.96[EUR][1000 genomes]
rs7073832	0.95[EUR][1000 genomes]
rs7076293	0.96[EUR][1000 genomes]
rs7082607	0.95[EUR][1000 genomes]
rs7084001	0.96[EUR][1000 genomes]
rs7085152	0.95[EUR][1000 genomes]
rs7086570	0.96[EUR][1000 genomes]
rs7088706	0.96[EUR][1000 genomes]
rs7089102	0.96[EUR][1000 genomes]
rs7089575	0.96[EUR][1000 genomes]
rs7093854	0.93[EUR][1000 genomes]
rs7094946	0.95[EUR][1000 genomes]
rs7097455	0.96[EUR][1000 genomes]
rs7098212	0.96[EUR][1000 genomes]
rs7099062	0.93[EUR][1000 genomes]
rs7100881	0.96[EUR][1000 genomes]
rs7477659	0.96[EUR][1000 genomes]
rs7896990	0.89[EUR][1000 genomes]
rs7897360	0.92[EUR][1000 genomes]
rs7898131	0.95[EUR][1000 genomes]
rs7899759	0.96[EUR][1000 genomes]
rs7900545	0.95[EUR][1000 genomes]
rs7900773	0.91[EUR][1000 genomes]
rs7901801	0.95[EUR][1000 genomes]
rs7910631	0.94[EUR][1000 genomes]
rs7910894	0.95[EUR][1000 genomes]
rs7911745	0.94[EUR][1000 genomes]
rs7912592	0.94[EUR][1000 genomes]
rs7913055	0.95[EUR][1000 genomes]
rs7913347	0.95[EUR][1000 genomes]
rs7913364	0.95[EUR][1000 genomes]
rs9299566	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9415397	0.94[EUR][1000 genomes]
rs9415405	0.96[EUR][1000 genomes]
rs9415406	0.96[EUR][1000 genomes]
rs9415410	0.94[EUR][1000 genomes]
rs9415412	0.94[EUR][1000 genomes]
rs9416445	0.81[EUR][1000 genomes]
rs9416447	0.94[EUR][1000 genomes]
rs9416449	0.94[EUR][1000 genomes]
rs9416451	0.95[EUR][1000 genomes]
rs9416452	0.95[EUR][1000 genomes]
rs9416458	0.95[EUR][1000 genomes]
rs9416461	0.96[EUR][1000 genomes]
rs9416462	0.96[EUR][1000 genomes]
rs9416465	0.96[EUR][1000 genomes]
rs9416467	0.96[EUR][1000 genomes]
rs9416469	0.95[EUR][1000 genomes]
rs9416470	0.96[EUR][1000 genomes]
rs9416473	0.95[EUR][1000 genomes]
rs9416474	0.94[EUR][1000 genomes]
rs9416475	0.94[EUR][1000 genomes]
rs9804235	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9804287	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9804334	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040047	chr10:57007182-57979747	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1051512	chr10:57470352-58026988	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv540645	chr10:57470352-58026988	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv971885	chr10:57727587-57893001	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv895501	chr10:57736009-57928768	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	esv2752691	chr10:57738694-58541894	Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
7	nsv895502	chr10:57747976-58099085	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	esv2750966	chr10:57754594-58023394	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv467257	chr10:57841516-57966330	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv551056	chr10:57841516-57966330	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:57826600-57850600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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