Variant report

Variant	rs2965636
Chromosome Location	chr7:52906693-52906694
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs12234825	0.81[EUR][1000 genomes]
rs12234864	0.81[EUR][1000 genomes]
rs2195134	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2912986	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2912987	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2912998	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2913009	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2913021	0.83[EUR][1000 genomes]
rs2913023	0.83[EUR][1000 genomes]
rs2913033	0.83[EUR][1000 genomes]
rs2913044	0.87[EUR][1000 genomes]
rs2913048	0.87[EUR][1000 genomes]
rs2913050	0.87[EUR][1000 genomes]
rs2965497	0.83[EUR][1000 genomes]
rs2965498	0.83[EUR][1000 genomes]
rs2965501	0.83[EUR][1000 genomes]
rs2965510	0.83[EUR][1000 genomes]
rs2965515	0.83[EUR][1000 genomes]
rs2965528	0.89[EUR][1000 genomes]
rs2965615	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2965628	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2965629	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2965640	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2965644	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2965662	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55640209	0.81[EUR][1000 genomes]
rs56345548	0.83[EUR][1000 genomes]
rs6951848	0.81[EUR][1000 genomes]
rs73106245	0.81[EUR][1000 genomes]
rs73106249	0.83[EUR][1000 genomes]
rs73699162	0.83[EUR][1000 genomes]
rs990236	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv888026	chr7:52588348-53013671	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv888027	chr7:52588348-53190508	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv888031	chr7:52797324-52944424	ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:52900400-52907000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:52905800-52907000	Enhancers	HUVEC	blood vessel
3	chr7:52906600-52907000	Enhancers	Muscle Satellite Cultured Cells	--
4	chr7:52906600-52907400	Enhancers	NH-A	brain

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