Variant report

Variant	rs1908166
Chromosome Location	chr11:25759132-25759133
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs1038932	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1038933	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1038934	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1038937	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1038938	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10501024	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10767439	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10767448	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10767449	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10767450	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10834774	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11028881	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11028888	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11028889	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11028890	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11028891	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11028892	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11028893	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11028903	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11028904	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11028905	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11028925	0.87[ASN][1000 genomes]
rs11028926	0.87[ASN][1000 genomes]
rs11028927	0.87[ASN][1000 genomes]
rs1121664	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1158052	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11601475	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12271018	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12271021	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12291285	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12360774	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12363608	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1493663	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1493676	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1493679	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1532287	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1532288	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1845335	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1908163	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1908164	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1908165	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1908167	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2131663	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2172581	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4923300	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4923303	0.84[ASN][1000 genomes]
rs4923304	0.81[ASN][1000 genomes]
rs4923305	0.84[ASN][1000 genomes]
rs56375749	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6484170	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6484171	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6484172	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7108839	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7127101	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7935615	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7935620	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7938971	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7939196	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7939236	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7944052	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9804685	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9804687	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs984830	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2760599	chr11:25186984-26159450	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1046507	chr11:25469712-26111707	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv2759811	chr11:25564190-25842666	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1041080	chr11:25585107-25931087	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1039190	chr11:25592509-25925352	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv540973	chr11:25592509-25925352	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1044636	chr11:25633583-25764193	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	esv2758259	chr11:25633803-25842666	Enhancers ZNF genes & repeats Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv428252	chr11:25633803-25842666	Enhancers ZNF genes & repeats Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv897137	chr11:25730008-25796742	Enhancers ZNF genes & repeats Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	esv1825232	chr11:25750628-25779039	Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:25757800-25759800	Enhancers	HepG2	liver

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