Variant report

Variant	rs7856657
Chromosome Location	chr9:15528567-15528568
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs1057644	1.00[ASN][1000 genomes]
rs1057645	1.00[ASN][1000 genomes]
rs1057646	1.00[ASN][1000 genomes]
rs10756687	0.83[LWK][hapmap]
rs10810392	0.80[AFR][1000 genomes]
rs10810394	0.80[AFR][1000 genomes]
rs10962048	0.90[CEU][hapmap]
rs12001969	1.00[ASN][1000 genomes]
rs12002581	1.00[ASN][1000 genomes]
rs12003712	1.00[ASN][1000 genomes]
rs1533040	0.83[LWK][hapmap]
rs16933212	0.85[YRI][hapmap]
rs16933257	1.00[ASN][1000 genomes]
rs16933296	0.90[CEU][hapmap];1.00[GIH][hapmap];0.88[TSI][hapmap]
rs16933317	0.85[YRI][hapmap]
rs16933326	0.92[YRI][hapmap]
rs16933330	0.91[YRI][hapmap]
rs16933332	1.00[ASN][1000 genomes]
rs16933350	0.90[CEU][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2175082	0.83[LWK][hapmap]
rs3087653	0.89[CEU][hapmap];1.00[GIH][hapmap];0.88[TSI][hapmap];0.83[EUR][1000 genomes]
rs41268961	0.83[EUR][1000 genomes]
rs41306098	0.83[EUR][1000 genomes]
rs4740615	0.83[LWK][hapmap]
rs57900433	1.00[ASN][1000 genomes]
rs58168894	0.86[AFR][1000 genomes]
rs59355275	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs59520337	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62570980	0.83[EUR][1000 genomes]
rs62570991	0.83[EUR][1000 genomes]
rs62570992	0.83[EUR][1000 genomes]
rs62570993	0.83[EUR][1000 genomes]
rs62571003	0.80[EUR][1000 genomes]
rs62571007	0.83[EUR][1000 genomes]
rs62571008	0.80[EUR][1000 genomes]
rs62571009	0.83[EUR][1000 genomes]
rs62571011	0.83[EUR][1000 genomes]
rs62571015	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62571016	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62571017	0.93[EUR][1000 genomes]
rs62571018	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62571029	0.88[EUR][1000 genomes]
rs62571033	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62571037	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62571046	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62571047	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62571048	0.97[EUR][1000 genomes]
rs62571050	0.90[EUR][1000 genomes]
rs62571051	0.88[EUR][1000 genomes]
rs62571052	0.85[EUR][1000 genomes]
rs7032720	1.00[ASN][1000 genomes]
rs72704750	1.00[ASN][1000 genomes]
rs73410204	0.91[AFR][1000 genomes]
rs73410215	0.86[AFR][1000 genomes]
rs73423305	1.00[ASN][1000 genomes]
rs7847771	0.90[YRI][hapmap]
rs7856486	1.00[ASN][1000 genomes]
rs7856523	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7857933	0.81[YRI][hapmap]
rs7858863	1.00[ASN][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	nsv517975	chr9:15286446-15534070	Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv892625	chr9:15326251-16064850	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv892626	chr9:15389610-15694690	Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv892627	chr9:15397969-15909450	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv892629	chr9:15516375-15634326	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15528400-15528800	Enhancers	GM12878-XiMat	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links