Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs13276608	0.91[AMR][1000 genomes]
rs17358602	1.00[ASN][1000 genomes]
rs34522585	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34618827	1.00[ASN][1000 genomes]
rs34885537	1.00[ASN][1000 genomes]
rs62519822	0.84[AMR][1000 genomes]
rs62519827	0.84[AMR][1000 genomes]
rs62519832	0.84[AMR][1000 genomes]
rs62519835	0.87[AMR][1000 genomes]
rs62519839	0.92[AMR][1000 genomes]
rs62519840	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62519841	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62519842	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62519843	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62519845	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62519847	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62519848	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62521079	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62521082	1.00[ASN][1000 genomes]
rs62521095	0.91[AMR][1000 genomes]
rs9650210	0.92[AMR][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	nsv534001	chr8:64992196-65798776	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
2	esv1847262	chr8:65509694-65595527	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv611449	chr8:65511032-65543401	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:65499800-65553000	Weak transcription	Pancreas	Pancrea
2	chr8:65503600-65538400	Weak transcription	Fetal Kidney	kidney
3	chr8:65517200-65540000	Weak transcription	Fetal Stomach	stomach
4	chr8:65517200-65540200	Weak transcription	Fetal Lung	lung
5	chr8:65517400-65535400	Weak transcription	Brain Anterior Caudate	brain
6	chr8:65517400-65540800	Weak transcription	Fetal Muscle Leg	muscle
7	chr8:65519000-65535200	Weak transcription	Ovary	ovary
8	chr8:65523200-65542400	Weak transcription	Primary hematopoietic stem cells	blood
9	chr8:65527800-65534800	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr8:65527800-65542400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr8:65528000-65530800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr8:65528000-65537600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr8:65528400-65530000	Weak transcription	Adipose Nuclei	Adipose
14	chr8:65528400-65535200	Weak transcription	Liver	Liver
15	chr8:65529200-65530000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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