Variant report

Variant	rs10464615
Chromosome Location	chr7:104328669-104328670
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10233987	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs10244859	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10279337	0.90[CHB][hapmap];0.85[JPT][hapmap]
rs10279375	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs11767604	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs11767619	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs12531723	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12534285	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12535033	1.00[CEU][hapmap];0.90[CHB][hapmap];0.88[YRI][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12536801	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12705261	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12705263	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12705264	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13241253	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13242612	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4255068	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4419737	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4496900	0.81[CHB][hapmap];0.83[JPT][hapmap]
rs4512324	0.91[CHB][hapmap];0.91[JPT][hapmap];0.81[ASN][1000 genomes]
rs4566971	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs4624947	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4730035	0.94[ASN][1000 genomes]
rs4730037	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs4730038	0.96[CEU][hapmap]
rs6944469	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs6945225	0.91[CHB][hapmap];0.91[JPT][hapmap];0.80[ASN][1000 genomes]
rs6952413	0.96[CEU][hapmap]
rs6962309	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6966224	0.93[CEU][hapmap]
rs7782285	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7801294	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9885990	0.86[CHB][hapmap];0.94[JPT][hapmap]
rs9886292	0.91[CHB][hapmap];1.00[JPT][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	nsv429790	chr7:104314049-104488049	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	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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