Variant report

Variant	rs2118891
Chromosome Location	chr2:212679643-212679644
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 91 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs10497950	1.00[CHB][hapmap];0.91[CHD][hapmap]
rs10497951	1.00[CHB][hapmap];0.91[CHD][hapmap];0.91[ASN][1000 genomes]
rs10804201	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs10932402	0.93[ASN][1000 genomes]
rs10932404	0.93[ASN][1000 genomes]
rs10932405	0.93[ASN][1000 genomes]
rs10932406	0.91[ASN][1000 genomes]
rs10932407	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs10932408	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs10932409	0.91[ASN][1000 genomes]
rs10932410	1.00[CHB][hapmap]
rs11885309	0.93[ASN][1000 genomes]
rs11887033	0.93[ASN][1000 genomes]
rs11887198	0.91[ASN][1000 genomes]
rs11892696	1.00[CHB][hapmap];0.91[CHD][hapmap];0.91[ASN][1000 genomes]
rs11894784	1.00[CHB][hapmap];0.88[CHD][hapmap];0.93[ASN][1000 genomes]
rs11894876	1.00[CHB][hapmap];0.93[ASN][1000 genomes]
rs11897941	0.93[ASN][1000 genomes]
rs11901045	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs11903196	0.91[ASN][1000 genomes]
rs12463864	1.00[CHB][hapmap]
rs12473270	0.93[ASN][1000 genomes]
rs12612277	0.93[ASN][1000 genomes]
rs12616558	0.93[ASN][1000 genomes]
rs12618183	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs12618478	1.00[CHB][hapmap];0.91[CHD][hapmap];0.93[ASN][1000 genomes]
rs12621282	1.00[CHB][hapmap]
rs12621800	0.93[ASN][1000 genomes]
rs12624020	0.91[ASN][1000 genomes]
rs12989469	1.00[CHB][hapmap];0.93[ASN][1000 genomes]
rs12993811	0.93[ASN][1000 genomes]
rs12998554	1.00[CHB][hapmap]
rs12999352	0.94[CHB][hapmap]
rs13002463	0.91[ASN][1000 genomes]
rs13002674	0.95[CHB][hapmap]
rs13005396	1.00[CHB][hapmap];0.88[JPT][hapmap]
rs13012677	1.00[CHB][hapmap];0.91[CHD][hapmap]
rs13019270	1.00[CHB][hapmap]
rs13021925	1.00[CHB][hapmap]
rs13022395	0.91[ASN][1000 genomes]
rs13024515	0.93[ASN][1000 genomes]
rs13024750	0.91[ASN][1000 genomes]
rs13025766	1.00[CHB][hapmap];0.88[JPT][hapmap]
rs13027991	0.91[ASN][1000 genomes]
rs13028597	1.00[CHB][hapmap]
rs13031164	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs13035912	1.00[CHB][hapmap]
rs1371199	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs1371200	1.00[CHB][hapmap];0.91[CHD][hapmap];0.89[JPT][hapmap]
rs1371201	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs1439233	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs1439234	1.00[CHB][hapmap];0.90[ASN][1000 genomes]
rs1439235	1.00[CHB][hapmap];0.91[CHD][hapmap];0.91[ASN][1000 genomes]
rs1439236	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs1439237	1.00[CHB][hapmap];0.93[ASN][1000 genomes]
rs1439238	0.93[ASN][1000 genomes]
rs1439240	0.91[ASN][1000 genomes]
rs1439241	0.93[ASN][1000 genomes]
rs1439242	1.00[CHB][hapmap];0.88[CHD][hapmap];0.93[ASN][1000 genomes]
rs1439243	0.93[ASN][1000 genomes]
rs1439254	1.00[CHB][hapmap]
rs16846873	1.00[CHB][hapmap];0.91[CHD][hapmap];0.89[JPT][hapmap];0.96[ASN][1000 genomes]
rs16846917	1.00[CHB][hapmap];0.91[CHD][hapmap];0.93[ASN][1000 genomes]
rs16847082	1.00[CHB][hapmap];0.87[JPT][hapmap]
rs16847087	0.80[JPT][hapmap]
rs16847160	0.84[CHB][hapmap]
rs34087388	0.97[ASN][1000 genomes]
rs34379058	0.97[ASN][1000 genomes]
rs35390180	0.93[ASN][1000 genomes]
rs35945815	0.93[ASN][1000 genomes]
rs36112432	0.93[ASN][1000 genomes]
rs4606869	1.00[CHB][hapmap];0.92[ASN][1000 genomes]
rs4673638	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs5006044	1.00[CHB][hapmap];0.85[JPT][hapmap]
rs56153935	0.93[ASN][1000 genomes]
rs59968041	0.93[ASN][1000 genomes]
rs67623637	0.97[ASN][1000 genomes]
rs67938035	0.97[ASN][1000 genomes]
rs68029722	0.93[ASN][1000 genomes]
rs714394	0.93[ASN][1000 genomes]
rs72948566	0.97[ASN][1000 genomes]
rs7565912	1.00[CHB][hapmap]
rs7570078	1.00[CHB][hapmap]
rs7589350	0.93[ASN][1000 genomes]
rs984773	1.00[CHB][hapmap]
rs991476	1.00[CHB][hapmap];0.91[CHD][hapmap];0.93[ASN][1000 genomes]
rs991477	1.00[CHB][hapmap];0.93[ASN][1000 genomes]
rs991495	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs991496	0.91[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	esv34128	chr2:212581485-212857122	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv875784	chr2:212639948-212761152	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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