Variant report

Variant	rs16934878
Chromosome Location	chr8:69577298-69577299
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:69576551..69578510-chr8:69582270..69584407,2	MCF-7	breast:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs11984995	0.85[AMR][1000 genomes]
rs11989752	0.82[YRI][hapmap]
rs11992298	0.82[CEU][hapmap];0.93[YRI][hapmap];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11993217	0.82[CEU][hapmap];0.81[YRI][hapmap]
rs11997399	0.83[EUR][1000 genomes]
rs16934892	0.94[YRI][hapmap]
rs16934901	1.00[CEU][hapmap]
rs16934903	0.82[YRI][hapmap]
rs16934930	0.82[CEU][hapmap];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs16934945	0.82[CEU][hapmap]
rs2676638	1.00[CEU][hapmap]
rs55691147	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs55718353	0.87[EUR][1000 genomes]
rs55731817	0.87[EUR][1000 genomes]
rs55820094	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs55851115	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs56194107	0.83[EUR][1000 genomes]
rs56405329	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs56706627	0.85[AMR][1000 genomes]
rs57624575	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs58619671	0.85[AMR][1000 genomes]
rs60577322	0.83[EUR][1000 genomes]
rs60704896	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs60946548	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6651316	0.87[AMR][1000 genomes]
rs6986385	0.82[CEU][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6987972	0.82[CEU][hapmap];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6992870	0.82[YRI][hapmap];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7012051	0.82[CEU][hapmap];0.87[EUR][1000 genomes]
rs7013783	0.82[CEU][hapmap];0.93[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73683589	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73683594	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73683595	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73683703	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7818845	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs984878	0.82[CEU][hapmap];0.83[EUR][1000 genomes]
rs9987198	0.87[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	chr8:69574800-69579600	Weak transcription	Aorta	Aorta
2	chr8:69577000-69577400	Weak transcription	NHDF-Ad	bronchial

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