Variant report

Variant	rs10836934
Chromosome Location	chr11:4930489-4930490
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10500627	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10500628	0.95[CHB][hapmap];0.95[JPT][hapmap];0.87[YRI][hapmap];0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10500629	0.86[CHB][hapmap];0.95[JPT][hapmap]
rs10500630	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs10742412	0.91[CHB][hapmap];0.95[JPT][hapmap]
rs10768355	0.91[CHB][hapmap];0.95[JPT][hapmap]
rs10836914	0.83[CHB][hapmap]
rs10836927	0.83[CHB][hapmap]
rs10836931	0.85[CEU][hapmap];0.96[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap]
rs10836932	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs10836935	0.85[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10836936	0.85[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11034546	0.83[CHB][hapmap]
rs11034573	1.00[CEU][hapmap];0.87[CHB][hapmap]
rs11034574	0.83[CHB][hapmap]
rs11034590	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs11034596	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11034602	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11034603	0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs12576085	0.87[CHB][hapmap]
rs12577475	0.83[CHB][hapmap]
rs1368831	0.85[CEU][hapmap];0.96[CHB][hapmap];0.91[JPT][hapmap]
rs16907254	0.82[JPT][hapmap]
rs7109669	0.91[CHB][hapmap];0.91[JPT][hapmap];0.95[ASN][1000 genomes]
rs9633907	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1054847	chr11:4642875-5200656	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
2	esv2758254	chr11:4907893-5135331	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
3	esv2759799	chr11:4907893-5135331	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
4	nsv896917	chr11:4917089-4935470	Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4930000-4930600	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr11:4930400-4930800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr11:4930400-4930800	Enhancers	Primary B cells from cord blood	blood
4	chr11:4930400-4931000	Enhancers	iPS-20b Cell Line	embryonic stem cell

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