Variant report

Variant	rs73128344
Chromosome Location	chr3:82043568-82043569
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12632087	1.00[AMR][1000 genomes]
rs6778193	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6778648	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73128312	1.00[ASN][1000 genomes]
rs73128314	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73128319	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73128324	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73128325	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73128327	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73128329	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73128348	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73128350	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73128352	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73130394	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73132331	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73133711	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73133730	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73133743	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73135722	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73135762	1.00[AMR][1000 genomes]
rs73136194	1.00[AMR][1000 genomes]
rs73136200	1.00[AMR][1000 genomes]
rs73138120	1.00[AMR][1000 genomes]
rs73138123	1.00[AMR][1000 genomes]
rs73138125	1.00[AMR][1000 genomes]
rs73138134	1.00[AMR][1000 genomes]
rs7635749	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7643979	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9872306	1.00[EUR][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:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:82039400-82046000	Weak transcription	HUES48 Cell Line	embryonic stem cell

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