Variant report

Variant	rs6970064
Chromosome Location	chr7:147202365-147202366
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10230324	0.82[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10952689	1.00[CEU][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs11762071	1.00[CEU][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs11765290	1.00[CEU][hapmap]
rs12703924	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap]
rs12703925	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs1528518	0.82[YRI][hapmap]
rs7792855	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7795843	1.00[CEU][hapmap]
rs7808124	1.00[CEU][hapmap]
rs7808274	1.00[CEU][hapmap];0.96[CHD][hapmap];0.91[GIH][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931005	chr7:146730472-147381257	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs6970064	OR2A5	cis	cerebellum	SCAN
rs6970064	GIMAP6	cis	cerebellum	SCAN

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

No data

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

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