Variant report

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1351363	1.00[ASN][1000 genomes]
rs16918927	1.00[EUR][1000 genomes]
rs16929168	1.00[EUR][1000 genomes]
rs16929206	1.00[EUR][1000 genomes]
rs16929234	1.00[EUR][1000 genomes]
rs16929308	1.00[EUR][1000 genomes]
rs16929351	1.00[EUR][1000 genomes]
rs16929371	1.00[EUR][1000 genomes]
rs16929390	1.00[EUR][1000 genomes]
rs16929420	1.00[ASN][1000 genomes]
rs16929430	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16929437	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2101043	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2101044	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2127581	1.00[EUR][1000 genomes]
rs28510229	1.00[ASN][1000 genomes]
rs57900808	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58717549	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60709086	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73256928	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73256936	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73256943	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73256979	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73264868	1.00[AMR][1000 genomes]
rs73264876	1.00[AMR][1000 genomes]
rs73264888	1.00[AMR][1000 genomes]
rs73264897	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73266909	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73266967	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018879	chr8:63281724-63937632	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv831340	chr8:63515126-63702660	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63648600-63649600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:63649200-63649600	Weak transcription	Adipose Nuclei	Adipose
3	chr8:63649200-63660200	Weak transcription	Cortex derived primary cultured neurospheres	brain

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