Variant report

Variant	rs7818845
Chromosome Location	chr8:69574999-69575000
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs11984995	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11989629	1.00[CEU][hapmap]
rs11989752	1.00[CEU][hapmap]
rs11992298	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11993217	1.00[CEU][hapmap]
rs11993687	1.00[CEU][hapmap]
rs11997399	1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes]
rs16934738	0.87[CEU][hapmap]
rs16934792	1.00[CEU][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes]
rs16934878	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs16934892	1.00[CEU][hapmap]
rs16934901	0.82[CEU][hapmap]
rs16934903	1.00[CEU][hapmap]
rs16934930	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16934945	1.00[CEU][hapmap]
rs16934954	1.00[CEU][hapmap]
rs17388090	1.00[CEU][hapmap]
rs2676638	0.82[CEU][hapmap]
rs55691147	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs55718353	0.96[EUR][1000 genomes]
rs55731817	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55820094	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs55821789	0.83[AMR][1000 genomes]
rs55851115	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56194107	0.92[EUR][1000 genomes]
rs56405329	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56706627	0.87[EUR][1000 genomes]
rs57624575	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58619671	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs59276657	0.87[EUR][1000 genomes]
rs60577322	0.92[EUR][1000 genomes]
rs60704896	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs60946548	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6651316	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs6986385	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6987972	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6991955	1.00[ASN][1000 genomes]
rs6992870	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7012051	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs7013783	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7014834	1.00[CEU][hapmap]
rs7015275	1.00[CEU][hapmap]
rs73683589	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73683594	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73683595	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73683703	0.96[EUR][1000 genomes]
rs7818791	1.00[CEU][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs984415	1.00[CEU][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes]
rs984878	1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes]
rs9987198	1.00[CEU][hapmap];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948687	chr8:69041121-69642540	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv890985	chr8:69532253-69586034	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv831349	chr8:69555461-69733515	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69569800-69575800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr8:69574800-69579600	Weak transcription	Aorta	Aorta

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