Variant report

Variant	rs10836931
Chromosome Location	chr11:4925500-4925501
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10500627	0.87[CEU][hapmap];0.96[CHB][hapmap];0.81[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10500628	1.00[CHB][hapmap];0.90[JPT][hapmap];0.88[YRI][hapmap];0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10500629	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs10500630	0.91[CHB][hapmap];0.85[JPT][hapmap]
rs10742412	0.95[CHB][hapmap];0.90[JPT][hapmap]
rs10768355	0.95[CHB][hapmap];0.90[JPT][hapmap]
rs10836914	0.87[CHB][hapmap]
rs10836927	0.88[CHB][hapmap]
rs10836932	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs10836934	0.85[CEU][hapmap];0.96[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10836935	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10836936	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11034546	0.88[CHB][hapmap]
rs11034554	0.84[CHB][hapmap]
rs11034573	0.87[CEU][hapmap];0.82[CHB][hapmap]
rs11034590	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs11034596	0.87[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11034602	0.87[CEU][hapmap];0.95[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11034603	0.91[CHB][hapmap];0.86[JPT][hapmap];0.95[ASN][1000 genomes]
rs12576085	0.82[CHB][hapmap]
rs12577475	0.88[CHB][hapmap]
rs1368831	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap]
rs4910692	0.83[CHB][hapmap]
rs7109669	0.95[CHB][hapmap];0.90[JPT][hapmap];0.98[ASN][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:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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