Variant report

Variant	rs7949547
Chromosome Location	chr11:84668923-84668924
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10792795	0.83[CHB][hapmap];0.85[YRI][hapmap]
rs10898338	0.91[CEU][hapmap];0.94[CHB][hapmap];0.87[JPT][hapmap];0.81[YRI][hapmap];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10898339	0.87[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10898341	0.94[CHB][hapmap];0.87[JPT][hapmap];0.93[YRI][hapmap]
rs11234253	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11234262	0.89[CHB][hapmap];0.90[YRI][hapmap]
rs11234263	0.94[CHB][hapmap];0.89[YRI][hapmap]
rs1470843	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17741917	0.96[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.82[YRI][hapmap];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1940130	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2374578	0.89[CHB][hapmap]
rs2444253	0.83[CHB][hapmap]
rs2508322	0.90[YRI][hapmap]
rs34813295	0.90[ASN][1000 genomes]
rs349063	0.80[YRI][hapmap]
rs349068	0.83[CHB][hapmap]
rs349069	0.83[CHB][hapmap]
rs349086	0.81[JPT][hapmap]
rs3851172	0.91[CEU][hapmap];0.94[CHB][hapmap];0.87[JPT][hapmap];0.81[YRI][hapmap];0.85[ASN][1000 genomes]
rs3851173	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs3851174	0.94[CHB][hapmap];0.87[JPT][hapmap];0.87[YRI][hapmap];0.83[ASN][1000 genomes]
rs3907015	0.85[YRI][hapmap]
rs3911270	0.91[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3911271	0.83[ASN][1000 genomes]
rs3911273	0.94[CHB][hapmap];0.87[JPT][hapmap];0.81[YRI][hapmap]
rs3933734	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs4121472	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs4121473	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs4271408	0.85[YRI][hapmap]
rs4943908	0.94[CHB][hapmap];0.87[JPT][hapmap];0.81[YRI][hapmap]
rs550970	0.89[CHB][hapmap];0.89[YRI][hapmap]
rs613972	0.83[YRI][hapmap]
rs619848	0.83[YRI][hapmap]
rs653885	0.80[YRI][hapmap]
rs6592218	0.89[CHB][hapmap]
rs6592219	0.89[CHB][hapmap];0.84[ASN][1000 genomes]
rs6592223	0.84[YRI][hapmap]
rs6592228	0.84[ASN][1000 genomes]
rs6592229	0.86[YRI][hapmap]
rs7105774	0.83[CHB][hapmap];0.93[YRI][hapmap]
rs7111336	0.90[YRI][hapmap]
rs7112064	0.94[CHB][hapmap];0.87[JPT][hapmap];0.87[YRI][hapmap]
rs7125600	0.89[CHB][hapmap];0.87[JPT][hapmap];0.93[YRI][hapmap]
rs7127826	1.00[CEU][hapmap];0.94[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7482922	0.94[CHB][hapmap];0.85[JPT][hapmap];0.93[YRI][hapmap]
rs7925898	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7929647	0.89[CHB][hapmap];0.84[YRI][hapmap]
rs7943194	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948410	chr11:83918339-84812001	Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1045974	chr11:84187214-84708462	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1048051	chr11:84419442-84784233	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv541109	chr11:84419442-84784233	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv898041	chr11:84642163-84722252	Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	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
7	nsv1054310	chr11:84661681-84702723	Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:84668800-84669000	Enhancers	Fetal Stomach	stomach

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