Variant report

Variant	rs7569836
Chromosome Location	chr2:67839751-67839752
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10182267	0.83[AMR][1000 genomes]
rs10184721	0.85[AMR][1000 genomes]
rs10187948	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10189868	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10189870	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10190391	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10197903	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10207162	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11883783	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11898758	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11904407	0.85[AMR][1000 genomes]
rs11904581	0.85[AMR][1000 genomes]
rs13387868	0.86[EUR][1000 genomes]
rs13398669	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13398896	0.82[CEU][hapmap]
rs13422158	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs58277478	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs60347662	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6706989	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6749548	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6761524	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72901828	0.97[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72901866	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7559840	1.00[CEU][hapmap];0.96[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7567910	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7568300	0.85[AMR][1000 genomes]
rs7569221	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7570412	0.85[AMR][1000 genomes]
rs7579880	0.83[AMR][1000 genomes]
rs7582772	0.85[AMR][1000 genomes]
rs7583557	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7594754	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7603152	1.00[CEU][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7604451	0.83[AMR][1000 genomes]
rs7607277	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]

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	nsv534389	chr2:67388428-68225338	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67839200-67840200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr2:67839200-67840800	Enhancers	Hela-S3	cervix
3	chr2:67839400-67840200	Enhancers	Placenta	Placenta
4	chr2:67839400-67840800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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