Variant report

Variant	rs56057734
Chromosome Location	chr11:62739633-62739634
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs11231281	0.82[AFR][1000 genomes]
rs11231282	0.81[AFR][1000 genomes]
rs11231283	0.83[AFR][1000 genomes]
rs11231291	0.84[AFR][1000 genomes]
rs11231292	0.84[AFR][1000 genomes]
rs11568621	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11568628	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11568629	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11828074	0.82[AFR][1000 genomes]
rs11828160	0.87[AFR][1000 genomes]
rs12293329	0.85[AFR][1000 genomes]
rs4077137	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56052738	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56192530	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56238281	0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56306952	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56406487	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57066277	0.83[AFR][1000 genomes]
rs57350702	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57932955	0.86[AFR][1000 genomes]
rs58244957	0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs60359411	0.87[AFR][1000 genomes]
rs61510834	0.87[AFR][1000 genomes]
rs67381592	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67406655	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67603137	0.85[AFR][1000 genomes]
rs7125335	0.83[AFR][1000 genomes]
rs7126908	0.81[AFR][1000 genomes]
rs72931384	1.00[ASN][1000 genomes]
rs72931390	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72931399	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72933422	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72933451	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72933455	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs736342	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7950683	0.82[AFR][1000 genomes]
rs947790	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532283	chr11:62201358-62863475	Enhancers Flanking Active TSS Genic enhancers Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1433 gene(s)	inside rSNPs	diseases
2	nsv1041770	chr11:62610353-62871767	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	263 gene(s)	inside rSNPs	diseases
3	esv34011	chr11:62652779-62993702	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 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	chr11:62728800-62742600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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