Variant report

Variant	rs11767619
Chromosome Location	chr7:104318103-104318104
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10233987	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10244859	0.86[CHB][hapmap];0.85[JPT][hapmap]
rs10279337	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10279375	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10464615	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs11767604	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs12531723	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs12536801	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs12705261	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs12705263	0.85[CHB][hapmap];0.85[JPT][hapmap]
rs12705264	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs13241253	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs13242612	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs4255068	0.85[CHB][hapmap];0.81[JPT][hapmap]
rs4419737	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs4512324	0.95[CHB][hapmap];0.90[JPT][hapmap];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4566971	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs4624947	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs4730037	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs6944469	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6945225	0.95[CHB][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs6955455	0.87[CHB][hapmap]
rs6962309	0.85[CHB][hapmap];0.83[JPT][hapmap]
rs9648932	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs9885990	0.86[CHB][hapmap]
rs9886292	0.86[CHB][hapmap];0.81[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv967437	chr7:104312412-104323208	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
2	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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