Variant report

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

rs_ID	r²[population]
rs6778193	1.00[ASN][1000 genomes]
rs6778648	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73128314	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73128319	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73128324	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73128325	1.00[ASN][1000 genomes]
rs73128327	1.00[ASN][1000 genomes]
rs73128329	1.00[ASN][1000 genomes]
rs73128344	1.00[ASN][1000 genomes]
rs73128348	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73128350	1.00[ASN][1000 genomes]
rs73128352	1.00[ASN][1000 genomes]
rs73130394	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73132331	1.00[ASN][1000 genomes]
rs73133711	1.00[ASN][1000 genomes]
rs73133730	1.00[ASN][1000 genomes]
rs73133743	1.00[ASN][1000 genomes]
rs73135722	1.00[ASN][1000 genomes]
rs7635749	1.00[ASN][1000 genomes]
rs7643979	1.00[ASN][1000 genomes]
rs9872306	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][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	esv2752870	chr3:82014410-82050310	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:82024400-82026800	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr3:82024400-82029800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr3:82024400-82030000	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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