Variant report

Variant	rs34892771
Chromosome Location	chr12:41781793-41781794
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10506191	0.89[EUR][1000 genomes]
rs10735995	0.83[ASN][1000 genomes]
rs10785235	0.87[EUR][1000 genomes]
rs10785259	0.91[EUR][1000 genomes]
rs10785261	0.91[EUR][1000 genomes]
rs10785262	0.98[EUR][1000 genomes]
rs10880054	0.88[EUR][1000 genomes]
rs10880063	0.89[EUR][1000 genomes]
rs10880071	0.98[EUR][1000 genomes]
rs11180834	0.85[EUR][1000 genomes]
rs11180836	0.88[EUR][1000 genomes]
rs11180843	0.89[EUR][1000 genomes]
rs11180851	0.89[EUR][1000 genomes]
rs11180878	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11614231	0.97[EUR][1000 genomes]
rs12146801	0.89[EUR][1000 genomes]
rs12369680	0.85[EUR][1000 genomes]
rs12370984	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12422274	0.88[EUR][1000 genomes]
rs12578784	0.89[EUR][1000 genomes]
rs12817575	0.89[EUR][1000 genomes]
rs1405549	0.89[EUR][1000 genomes]
rs1458176	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1527090	0.88[EUR][1000 genomes]
rs1534279	0.88[EUR][1000 genomes]
rs1534280	0.89[EUR][1000 genomes]
rs1544000	0.89[EUR][1000 genomes]
rs1902907	0.85[EUR][1000 genomes]
rs1902909	0.91[EUR][1000 genomes]
rs1902911	0.91[EUR][1000 genomes]
rs1918221	0.89[EUR][1000 genomes]
rs1918226	0.89[EUR][1000 genomes]
rs1918227	0.89[EUR][1000 genomes]
rs2199030	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2405911	0.89[EUR][1000 genomes]
rs2897268	0.89[EUR][1000 genomes]
rs34220247	0.88[EUR][1000 genomes]
rs6582332	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6582334	0.89[EUR][1000 genomes]
rs6582336	0.87[EUR][1000 genomes]
rs7301366	0.90[EUR][1000 genomes]
rs7315276	0.91[EUR][1000 genomes]
rs7488531	0.88[EUR][1000 genomes]
rs7956320	0.88[EUR][1000 genomes]
rs7956499	0.81[ASN][1000 genomes]
rs7957823	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7960955	0.90[EUR][1000 genomes]
rs7967532	0.91[EUR][1000 genomes]
rs7979586	0.89[EUR][1000 genomes]
rs930905	0.89[EUR][1000 genomes]
rs961337	0.88[EUR][1000 genomes]
rs9783512	0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832383	chr12:41693298-41846934	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
2	nsv832384	chr12:41772648-41971430	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv899036	chr12:41777144-41807859	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	n/a
4	nsv899037	chr12:41777144-41819215	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	n/a
5	nsv1044910	chr12:41778831-41813198	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	n/a
6	esv2761735	chr12:41780758-41811938	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	n/a
7	esv2757501	chr12:41780758-41816002	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	n/a
8	esv2759896	chr12:41780758-41816002	Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	n/a
9	esv2755020	chr12:41780758-41820936	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:41776200-41787400	Weak transcription	Aorta	Aorta

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