Variant report

Variant	rs349084
Chromosome Location	chr11:84812624-84812625
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10792795	1.00[CEU][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.86[YRI][hapmap]
rs10792796	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10898341	1.00[CEU][hapmap];0.82[YRI][hapmap]
rs11234262	1.00[CEU][hapmap];0.80[CHB][hapmap];0.82[YRI][hapmap];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11234263	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.82[YRI][hapmap];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11234269	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2374578	0.96[CEU][hapmap];0.84[TSI][hapmap]
rs2444253	0.83[CHB][hapmap];0.82[ASN][1000 genomes]
rs2508322	0.82[YRI][hapmap]
rs34813295	0.84[EUR][1000 genomes]
rs349057	0.85[CEU][hapmap];0.95[GIH][hapmap];0.91[MEX][hapmap];0.91[TSI][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs349060	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs349063	0.86[YRI][hapmap];0.82[AFR][1000 genomes]
rs349068	0.82[CHB][hapmap]
rs349069	0.94[CHB][hapmap];0.86[JPT][hapmap];0.86[YRI][hapmap]
rs349076	0.88[CEU][hapmap];0.83[MKK][hapmap];0.80[AMR][1000 genomes]
rs349078	1.00[CEU][hapmap];0.82[CHB][hapmap];0.89[JPT][hapmap];0.88[YRI][hapmap];0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs349080	1.00[CEU][hapmap];0.84[CHB][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs349082	1.00[CEU][hapmap];0.89[CHB][hapmap];0.84[JPT][hapmap];0.89[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs349083	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs349085	0.88[CEU][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap]
rs349086	0.96[CEU][hapmap];0.94[CHB][hapmap];0.96[YRI][hapmap]
rs349089	0.96[CEU][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3844142	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs3851173	0.96[CEU][hapmap];0.89[TSI][hapmap]
rs3851174	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs3862780	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3862781	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3907015	1.00[CEU][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.86[YRI][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3911271	0.80[AMR][1000 genomes]
rs3911273	0.96[CEU][hapmap]
rs4271408	0.88[CHB][hapmap];0.82[JPT][hapmap]
rs4943908	0.96[CEU][hapmap]
rs4944509	0.85[ASN][1000 genomes]
rs506422	0.82[YRI][hapmap]
rs550970	0.81[TSI][hapmap];0.82[YRI][hapmap]
rs573767	0.81[TSI][hapmap];0.86[YRI][hapmap]
rs582399	0.86[ASN][1000 genomes]
rs613972	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs616320	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs619848	1.00[CEU][hapmap];0.82[CHB][hapmap]
rs630015	1.00[CEU][hapmap]
rs634050	0.89[CHB][hapmap];0.82[MKK][hapmap];0.86[YRI][hapmap];0.81[ASN][1000 genomes]
rs635860	0.86[YRI][hapmap]
rs652852	0.88[CHB][hapmap];0.85[JPT][hapmap];0.86[YRI][hapmap];0.88[ASN][1000 genomes]
rs653885	0.86[YRI][hapmap]
rs6592218	0.96[CEU][hapmap]
rs6592219	0.96[CEU][hapmap]
rs6592229	1.00[CEU][hapmap];0.85[YRI][hapmap]
rs7105774	1.00[CEU][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap]
rs7111336	1.00[CEU][hapmap];0.82[YRI][hapmap]
rs7112064	1.00[CEU][hapmap];0.86[YRI][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7125600	1.00[CEU][hapmap]
rs7131501	1.00[CEU][hapmap];0.83[CHB][hapmap];0.95[GIH][hapmap];0.90[MEX][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7131533	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7482922	0.82[CHB][hapmap]
rs7929647	1.00[CEU][hapmap];0.80[CHB][hapmap];0.86[YRI][hapmap]
rs7931733	1.00[CEU][hapmap];0.86[YRI][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7933636	0.93[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430415	chr11:84661652-84833852	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1040393	chr11:84708402-84866594	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv527535	chr11:84724795-84895033	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv528491	chr11:84724795-84895033	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv1044370	chr11:84748993-85293233	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 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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