Variant report

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs13378951	1.00[EUR][1000 genomes]
rs16953949	1.00[EUR][1000 genomes]
rs28488241	1.00[EUR][1000 genomes]
rs4053687	1.00[EUR][1000 genomes]
rs7317397	1.00[EUR][1000 genomes]
rs7319368	0.84[AFR][1000 genomes]
rs7324834	0.85[AFR][1000 genomes]
rs7325474	0.90[YRI][hapmap];0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7328024	0.87[AMR][1000 genomes]
rs73549299	1.00[EUR][1000 genomes]
rs73550844	0.87[AMR][1000 genomes]
rs7492110	1.00[EUR][1000 genomes]
rs7983514	0.87[AMR][1000 genomes]
rs7986614	0.87[AMR][1000 genomes]
rs7987624	0.87[AMR][1000 genomes]
rs7998889	1.00[YRI][hapmap]
rs9300371	1.00[EUR][1000 genomes]
rs9300381	1.00[EUR][1000 genomes]
rs9300383	0.87[AMR][1000 genomes]
rs9300388	1.00[EUR][1000 genomes]
rs9300390	1.00[EUR][1000 genomes]
rs9300391	1.00[EUR][1000 genomes]
rs9582078	1.00[EUR][1000 genomes]
rs9582111	1.00[EUR][1000 genomes]
rs9582112	1.00[EUR][1000 genomes]
rs9582113	1.00[EUR][1000 genomes]
rs9582114	1.00[EUR][1000 genomes]
rs9582119	1.00[EUR][1000 genomes]
rs9582120	1.00[EUR][1000 genomes]
rs9584460	1.00[EUR][1000 genomes]
rs9584486	0.91[AFR][1000 genomes]
rs9584488	1.00[EUR][1000 genomes]
rs9584503	1.00[EUR][1000 genomes]
rs9584504	1.00[EUR][1000 genomes]
rs9584508	1.00[EUR][1000 genomes]
rs9584514	1.00[EUR][1000 genomes]
rs9584519	1.00[EUR][1000 genomes]
rs9584521	1.00[EUR][1000 genomes]
rs9584523	1.00[EUR][1000 genomes]
rs9584525	1.00[EUR][1000 genomes]
rs9584531	1.00[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	nsv832693	chr13:97594845-97777481	Bivalent/Poised TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr13:97695000-97696400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr13:97695000-97696400	Enhancers	HUVEC	blood vessel
3	chr13:97695200-97696400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr13:97695600-97696400	Enhancers	Fetal Brain Male	brain

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