Variant report

Variant	rs6656405
Chromosome Location	chr1:216181480-216181481
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10779662	1.00[CEU][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10779663	1.00[CEU][hapmap];0.82[YRI][hapmap]
rs10864217	0.92[CEU][hapmap];0.92[JPT][hapmap];0.86[EUR][1000 genomes]
rs10864219	0.89[CEU][hapmap];0.93[CHB][hapmap];0.92[JPT][hapmap];0.95[MEX][hapmap];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10864220	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10864222	0.86[AMR][1000 genomes]
rs10864226	0.84[CEU][hapmap];0.91[MEX][hapmap];0.84[TSI][hapmap]
rs11120706	0.86[EUR][1000 genomes]
rs11120707	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11120709	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11120711	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11120712	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11120713	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11120719	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11120725	0.96[CEU][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12034192	0.86[AMR][1000 genomes]
rs12049048	1.00[CEU][hapmap];0.82[YRI][hapmap]
rs12084647	1.00[CEU][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12566058	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12736533	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1561173	1.00[CEU][hapmap];0.82[YRI][hapmap]
rs2164577	0.87[EUR][1000 genomes]
rs28658221	0.98[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4471233	0.96[CEU][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4501816	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4503324	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4655293	0.98[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4655440	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs571926	0.86[CHB][hapmap];0.92[JPT][hapmap];0.81[ASN][1000 genomes]
rs6696269	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7531584	0.92[CEU][hapmap];1.00[CHB][hapmap];0.90[GIH][hapmap];0.92[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7541086	0.92[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006504	chr1:215890460-216642124	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv535288	chr1:215890460-216642124	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv428599	chr1:216086224-216267211	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv873172	chr1:216144827-216281673	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv873173	chr1:216151789-216204488	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv873174	chr1:216151789-216211989	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region lncRNA	1 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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