Variant report

Variant	rs10957889
Chromosome Location	chr8:79331394-79331395
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10957890	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11775617	0.84[EUR][1000 genomes]
rs11776326	0.86[EUR][1000 genomes]
rs11782530	0.82[EUR][1000 genomes]
rs11997760	0.85[EUR][1000 genomes]
rs11997999	0.85[EUR][1000 genomes]
rs12679807	0.86[EUR][1000 genomes]
rs13248210	0.82[EUR][1000 genomes]
rs13257652	0.82[EUR][1000 genomes]
rs13262571	0.85[EUR][1000 genomes]
rs13267958	0.85[EUR][1000 genomes]
rs13267990	0.85[EUR][1000 genomes]
rs13268612	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13269738	0.86[EUR][1000 genomes]
rs13271734	0.85[EUR][1000 genomes]
rs13273641	0.87[EUR][1000 genomes]
rs13274037	0.84[EUR][1000 genomes]
rs13274739	0.85[EUR][1000 genomes]
rs13275132	0.86[EUR][1000 genomes]
rs13278555	0.85[EUR][1000 genomes]
rs4413764	0.85[EUR][1000 genomes]
rs4527861	0.86[EUR][1000 genomes]
rs62519510	0.85[EUR][1000 genomes]
rs6473098	0.85[EUR][1000 genomes]
rs6473099	0.85[EUR][1000 genomes]
rs6473100	0.85[EUR][1000 genomes]
rs6473101	0.84[EUR][1000 genomes]
rs6473102	1.00[ASN][1000 genomes]
rs6995111	0.85[EUR][1000 genomes]
rs6996260	0.86[EUR][1000 genomes]
rs6997037	0.87[EUR][1000 genomes]
rs7012638	0.85[EUR][1000 genomes]
rs7013188	0.85[EUR][1000 genomes]
rs7013333	0.85[EUR][1000 genomes]
rs7016593	0.86[EUR][1000 genomes]
rs7018296	0.85[EUR][1000 genomes]
rs7827766	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7830219	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7831788	0.85[EUR][1000 genomes]
rs7844386	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891056	chr8:79206819-79394667	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1017218	chr8:79287819-79434844	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv539652	chr8:79287819-79434844	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1033453	chr8:79320533-79485680	Active TSS Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:79326400-79331800	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chr8:79330400-79331400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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