Variant report

Variant	rs9767586
Chromosome Location	chr6:70635536-70635537
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10428870	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1417577	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1547783	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16868360	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17689265	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17689448	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17709736	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17745952	0.88[EUR][1000 genomes]
rs2096059	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2096060	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2096061	0.88[EUR][1000 genomes]
rs2345783	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56163905	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56978419	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57358062	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs60536675	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6901568	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6903986	1.00[ASN][1000 genomes]
rs6929367	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73480069	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7747604	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9446176	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9454918	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9454920	0.91[EUR][1000 genomes];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	nsv886140	chr6:70354682-70728202	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv886141	chr6:70590638-70694162	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1026151	chr6:70621616-70946967	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv463151	chr6:70625166-70694162	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv603636	chr6:70625166-70694162	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:70625600-70642200	Weak transcription	Fetal Heart	heart
2	chr6:70634000-70636000	Weak transcription	Primary B cells from cord blood	blood
3	chr6:70634000-70636000	Weak transcription	Primary B cells from peripheral blood	blood
4	chr6:70634000-70636000	Weak transcription	GM12878-XiMat	blood

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