Variant report

Variant	rs7935726
Chromosome Location	chr11:18246943-18246944
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10766463	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10832904	0.85[CEU][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10832908	0.96[CEU][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11024553	0.88[CEU][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11024561	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11024562	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11024563	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11024566	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11024574	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11024576	0.81[CEU][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes]
rs11024577	1.00[JPT][hapmap]
rs11024578	0.96[CEU][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11601002	0.82[AMR][1000 genomes]
rs12361253	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12364058	0.88[CEU][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12364776	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12791694	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs1915391	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2168363	0.96[CEU][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2445145	0.86[EUR][1000 genomes]
rs2445175	0.88[CEU][hapmap];0.83[EUR][1000 genomes]
rs2445176	0.85[EUR][1000 genomes]
rs2445225	0.84[EUR][1000 genomes]
rs2445226	0.84[EUR][1000 genomes]
rs2460831	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2468779	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2468790	0.86[CEU][hapmap];0.85[EUR][1000 genomes]
rs2468856	0.88[EUR][1000 genomes]
rs2925145	0.85[EUR][1000 genomes]
rs4757627	0.85[CEU][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4757628	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4757629	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4757630	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56310011	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs67006796	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs67712345	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7103794	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7117484	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7117890	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72881516	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949248	chr11:17791822-18692687	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
2	nsv428569	chr11:18194030-18350869	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18244600-18247000	Enhancers	Liver	Liver
2	chr11:18246600-18249400	Enhancers	Primary B cells from peripheral blood	blood
3	chr11:18246800-18250400	Weak transcription	HepG2	liver

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