Variant report

Variant	rs7646696
Chromosome Location	chr3:144204743-144204744
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs11926933	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12106820	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs34217903	0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs34892796	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs35118386	0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs35127961	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs35691495	0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs35817971	0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs35986789	0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs56165545	0.92[ASN][1000 genomes]
rs56902722	0.92[ASN][1000 genomes]
rs56975803	0.92[ASN][1000 genomes]
rs57544326	0.92[ASN][1000 genomes]
rs57959140	0.93[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs58424525	0.92[ASN][1000 genomes]
rs58805587	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs58982449	0.92[ASN][1000 genomes]
rs60261236	0.92[ASN][1000 genomes]
rs66899526	0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6763485	0.93[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs67706818	0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6778932	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73009071	0.92[ASN][1000 genomes]
rs73009079	0.92[ASN][1000 genomes]
rs73011007	0.92[ASN][1000 genomes]
rs73011009	0.92[ASN][1000 genomes]
rs73011013	0.92[ASN][1000 genomes]
rs73011015	0.92[ASN][1000 genomes]
rs73011028	0.92[ASN][1000 genomes]
rs73011034	0.92[ASN][1000 genomes]
rs73871203	0.88[ASN][1000 genomes]
rs73875129	0.92[ASN][1000 genomes]
rs73875142	0.92[ASN][1000 genomes]
rs7610158	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7614112	0.92[ASN][1000 genomes]
rs7614176	0.92[ASN][1000 genomes]
rs7614241	0.92[ASN][1000 genomes]
rs7620185	0.92[ASN][1000 genomes]
rs7629865	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7629872	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7636124	0.92[ASN][1000 genomes]
rs7641994	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532633	chr3:143802417-144440646	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1011685	chr3:143959237-144218424	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv536751	chr3:143959237-144218424	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv591928	chr3:144050897-144822081	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv2756108	chr3:144177836-144301659	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv877571	chr3:144188561-144291254	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:144203400-144208000	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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