Variant report

Variant	rs4853267
Chromosome Location	chr2:76967644-76967645
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10179084	0.90[EUR][1000 genomes]
rs10181947	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11682401	0.88[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs12232994	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12713879	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12993991	0.89[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs12994214	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs13406374	0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs17013121	0.95[ASN][1000 genomes]
rs2056207	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2056208	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2056209	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2056210	0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2056211	0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2056212	0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2056213	0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs28419312	0.81[EUR][1000 genomes]
rs2860832	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4322873	0.80[EUR][1000 genomes]
rs4853268	0.81[EUR][1000 genomes]
rs4853269	0.81[EUR][1000 genomes]
rs55678874	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs61283380	0.81[EUR][1000 genomes]
rs6726562	0.89[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs6730814	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6745704	0.96[ASN][1000 genomes]
rs6750387	0.92[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7559330	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7569282	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7584499	0.90[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7585902	0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7595233	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs969933	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs969934	0.95[ASN][1000 genomes]
rs971121	0.90[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs973370	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs973371	0.91[AMR][1000 genomes];1.00[ASN][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	nsv582235	chr2:76881210-76997763	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv874319	chr2:76949101-76979415	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:76960800-76974600	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr2:76963800-76985800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr2:76967600-76968000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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