Variant report

Variant	rs16847874
Chromosome Location	chr2:213066035-213066036
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10804203	1.00[CEU][hapmap]
rs10932424	1.00[CEU][hapmap]
rs10932427	1.00[CEU][hapmap]
rs1467273	1.00[CEU][hapmap]
rs1467275	1.00[CEU][hapmap]
rs1521635	0.88[EUR][1000 genomes]
rs1521637	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs1568516	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs16848072	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs16848106	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs16848142	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs16848151	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs17345590	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17346524	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs17346678	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs17346733	1.00[CEU][hapmap]
rs17417710	1.00[CEU][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17418160	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs17418250	1.00[YRI][hapmap]
rs17418591	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs17418884	1.00[CEU][hapmap]
rs17419114	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs1915743	1.00[CEU][hapmap]
rs2371569	1.00[CEU][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55921734	0.80[EUR][1000 genomes]
rs73066368	0.80[EUR][1000 genomes]
rs7572084	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs7572366	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs7572462	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs7586610	1.00[CEU][hapmap];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011572	chr2:212840066-213152279	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv875805	chr2:212891401-213164837	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv875806	chr2:212997024-213211067	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1001718	chr2:213047033-213155985	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1004823	chr2:213052804-213181263	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv536138	chr2:213052804-213181263	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1006051	chr2:213052804-213273642	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv875807	chr2:213054058-213103721	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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