Variant report

Variant	rs11719361
Chromosome Location	chr3:22745754-22745755
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10446448	0.82[ASN][1000 genomes]
rs11715788	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11718398	0.82[ASN][1000 genomes]
rs12107774	0.81[EUR][1000 genomes]
rs12715040	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13066404	0.82[ASN][1000 genomes]
rs13085397	0.82[ASN][1000 genomes]
rs13085538	0.82[ASN][1000 genomes]
rs13085890	0.82[EUR][1000 genomes]
rs13087228	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13092639	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13094040	0.82[ASN][1000 genomes]
rs13094117	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13100238	0.82[ASN][1000 genomes]
rs1597454	0.82[ASN][1000 genomes]
rs17337351	0.82[ASN][1000 genomes]
rs17395804	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17396388	0.82[ASN][1000 genomes]
rs34065935	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35342568	0.82[ASN][1000 genomes]
rs35801066	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs36004686	0.82[ASN][1000 genomes]
rs36046005	0.84[EUR][1000 genomes]
rs67445281	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9878458	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460477	chr3:22532660-22920246	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv589941	chr3:22532660-22920246	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1014828	chr3:22554271-23033498	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1012343	chr3:22560733-22811382	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv589946	chr3:22600086-22865347	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1007224	chr3:22612682-22809139	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv536522	chr3:22612682-22809139	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1011446	chr3:22612682-22864885	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr3:22745600-22746200	Enhancers	Monocytes-CD14+_RO01746	blood

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