Variant report

Variant	rs34848022
Chromosome Location	chr6:65210797-65210798
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10494882	0.87[EUR][1000 genomes]
rs10494883	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10626520	0.83[EUR][1000 genomes]
rs11751191	0.88[ASN][1000 genomes]
rs11758090	0.88[ASN][1000 genomes]
rs11759853	0.88[ASN][1000 genomes]
rs13193668	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13194506	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13199165	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13202092	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13212221	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13212239	0.97[EUR][1000 genomes]
rs13212470	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13212894	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13218626	0.98[EUR][1000 genomes]
rs1337511	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1337512	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1337519	0.93[EUR][1000 genomes]
rs1337520	0.93[EUR][1000 genomes]
rs1361261	0.88[ASN][1000 genomes]
rs16895262	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs16895263	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs16895281	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs16895329	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs16895338	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16895394	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1890471	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34204982	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35014638	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3846796	0.85[EUR][1000 genomes]
rs3846797	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3904796	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4710478	0.88[ASN][1000 genomes]
rs594182	0.87[EUR][1000 genomes]
rs6920553	0.91[EUR][1000 genomes]
rs72874924	0.89[EUR][1000 genomes]
rs7746514	0.91[EUR][1000 genomes]
rs9342288	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9342308	0.96[EUR][1000 genomes]
rs9342310	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9345146	0.85[EUR][1000 genomes]
rs9345178	0.84[EUR][1000 genomes]
rs9345179	0.87[EUR][1000 genomes]
rs9345180	0.87[EUR][1000 genomes]
rs9345182	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9351272	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9351287	0.87[EUR][1000 genomes]
rs9351291	0.91[EUR][1000 genomes]
rs9353864	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9353865	0.87[EUR][1000 genomes]
rs9353869	0.98[EUR][1000 genomes]
rs9359957	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9359958	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9359962	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9362900	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9362901	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9362909	0.87[EUR][1000 genomes]
rs9362916	0.86[EUR][1000 genomes]
rs9362922	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9451826	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026162	chr6:64639580-65470828	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv538272	chr6:64639580-65470828	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1015718	chr6:64821273-65479726	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv885999	chr6:64946169-65227097	Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv830675	chr6:65034132-65223344	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1018075	chr6:65185962-65234866	Enhancers Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
7	nsv1021566	chr6:65186049-65229208	Weak transcription Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:65207600-65213000	Weak transcription	Fetal Lung	lung
2	chr6:65208400-65212600	Weak transcription	HUVEC	blood vessel

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