Variant report

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs16931279	1.00[EUR][1000 genomes]
rs55730348	1.00[EUR][1000 genomes]
rs58668300	1.00[EUR][1000 genomes]
rs58715144	1.00[EUR][1000 genomes]
rs58897334	1.00[EUR][1000 genomes]
rs59355904	1.00[EUR][1000 genomes]
rs6988434	1.00[EUR][1000 genomes]
rs6994261	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7003587	1.00[EUR][1000 genomes]
rs73234031	1.00[EUR][1000 genomes]
rs73234094	1.00[EUR][1000 genomes]
rs73237705	1.00[EUR][1000 genomes]
rs73237734	1.00[EUR][1000 genomes]
rs73237742	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73237746	1.00[EUR][1000 genomes]
rs73237756	1.00[EUR][1000 genomes]
rs73237764	1.00[EUR][1000 genomes]
rs73237765	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73246200	1.00[EUR][1000 genomes]
rs73248315	1.00[EUR][1000 genomes]
rs73248316	1.00[EUR][1000 genomes]
rs73248341	1.00[EUR][1000 genomes]
rs73248376	1.00[EUR][1000 genomes]
rs73689571	1.00[EUR][1000 genomes]
rs7817370	1.00[EUR][1000 genomes]
rs7821719	1.00[EUR][1000 genomes]
rs7827701	1.00[EUR][1000 genomes]
rs7832640	1.00[EUR][1000 genomes]
rs7833820	1.00[EUR][1000 genomes]
rs9694711	1.00[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	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:14 , 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	chr8:65528400-65535200	Weak transcription	Liver	Liver
14	chr8:65530000-65539800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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