Variant report

Variant	rs13022306
Chromosome Location	chr2:212718480-212718481
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 103 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:98)

rs_ID	r²[population]
rs10497950	1.00[CEU][hapmap]
rs10497951	1.00[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10497952	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10804201	1.00[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10932402	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10932404	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10932405	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10932406	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10932407	1.00[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10932408	1.00[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10932409	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10932410	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs11679499	1.00[CHB][hapmap]
rs11885309	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11887033	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11887198	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11892696	1.00[CEU][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11893981	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11894784	1.00[CEU][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11894876	0.93[CEU][hapmap];0.91[YRI][hapmap];0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11897941	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11901045	1.00[CEU][hapmap]
rs11903196	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12463864	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs12473270	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12612277	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12616558	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12618183	1.00[CEU][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12618478	1.00[CEU][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12621282	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs12621800	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12624020	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12989469	1.00[CEU][hapmap];0.91[YRI][hapmap];0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12991661	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap]
rs12992022	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap]
rs12993811	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12996321	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12998554	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs12999352	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs13002463	1.00[CEU][hapmap];0.90[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13002674	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs13003524	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13005396	1.00[CEU][hapmap]
rs13012677	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs13019270	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs13021925	0.93[CEU][hapmap];1.00[YRI][hapmap]
rs13022395	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13024515	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13024750	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13025766	1.00[CEU][hapmap]
rs13027991	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13028597	1.00[CEU][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap]
rs13029024	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs13031164	1.00[CEU][hapmap]
rs13035912	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs1371199	1.00[CEU][hapmap]
rs1371200	1.00[CEU][hapmap]
rs1371201	1.00[CEU][hapmap]
rs1439233	1.00[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1439234	1.00[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1439235	1.00[CEU][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1439236	0.90[CEU][hapmap];0.92[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1439237	1.00[CEU][hapmap];0.91[YRI][hapmap];0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1439238	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1439240	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1439241	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1439242	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1439243	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1439254	1.00[CEU][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap]
rs16846873	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs16846917	1.00[YRI][hapmap]
rs16847082	1.00[CEU][hapmap]
rs16847087	0.86[CEU][hapmap]
rs16847122	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap]
rs16847160	0.93[CEU][hapmap]
rs34087388	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34379058	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35390180	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35945815	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs36112432	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4606869	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4673638	1.00[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs5006044	0.86[CEU][hapmap];0.80[JPT][hapmap];0.91[YRI][hapmap]
rs56153935	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs59968041	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs67623637	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs67938035	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs68029722	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs714394	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72948566	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7565912	1.00[CEU][hapmap];0.91[YRI][hapmap]
rs7570078	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs7589350	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs984773	0.91[YRI][hapmap]
rs991476	1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs991477	1.00[CEU][hapmap];0.83[YRI][hapmap];0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs991495	0.89[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs991496	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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
3	nsv875785	chr2:212683946-212752193	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
4	nsv834525	chr2:212693190-212860356	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv875786	chr2:212715410-212752193	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No data

Quick Search:

Input of quick search could be:

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

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links