Variant report

Variant	rs9589612
Chromosome Location	chr13:93309185-93309186
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10507991	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10507992	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10507993	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11842192	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12323119	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12583136	0.81[EUR][1000 genomes]
rs12583839	0.81[EUR][1000 genomes]
rs12583849	0.81[EUR][1000 genomes]
rs12866354	0.81[EUR][1000 genomes]
rs12869086	0.80[EUR][1000 genomes]
rs12875094	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12875257	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12875425	0.80[EUR][1000 genomes]
rs12875722	0.80[EUR][1000 genomes]
rs12877956	0.80[EUR][1000 genomes]
rs1316999	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17188529	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17188536	0.92[ASN][1000 genomes]
rs17188543	0.80[EUR][1000 genomes]
rs17188557	0.81[EUR][1000 genomes]
rs17188564	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs17188578	0.80[EUR][1000 genomes]
rs17188599	0.80[EUR][1000 genomes]
rs17188606	0.80[EUR][1000 genomes]
rs17267292	0.81[EUR][1000 genomes]
rs17267306	0.80[EUR][1000 genomes]
rs1933183	0.80[EUR][1000 genomes]
rs1933184	0.80[EUR][1000 genomes]
rs1933185	0.80[EUR][1000 genomes]
rs1933186	0.81[EUR][1000 genomes]
rs2152926	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs33953114	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34065542	0.80[EUR][1000 genomes]
rs34378377	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34469781	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34521935	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34715171	0.80[EUR][1000 genomes]
rs34783515	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34864437	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34956289	0.81[EUR][1000 genomes]
rs34989016	0.80[EUR][1000 genomes]
rs35206958	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35391103	0.80[EUR][1000 genomes]
rs35478536	0.81[EUR][1000 genomes]
rs35871738	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35888127	0.80[EUR][1000 genomes]
rs4418924	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4459436	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61974463	0.80[EUR][1000 genomes]
rs61974465	0.80[EUR][1000 genomes]
rs61974466	0.80[EUR][1000 genomes]
rs61974467	0.80[EUR][1000 genomes]
rs61975922	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs61975923	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs61975924	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61975929	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61975930	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61975931	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61975932	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61975933	0.81[EUR][1000 genomes]
rs61975934	0.80[EUR][1000 genomes]
rs61975937	0.80[EUR][1000 genomes]
rs61975942	0.81[EUR][1000 genomes]
rs61975943	0.80[EUR][1000 genomes]
rs61975944	0.80[EUR][1000 genomes]
rs71427588	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045395	chr13:93248456-93323269	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv456071	chr13:93279563-93377562	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv562745	chr13:93279563-93377562	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv18734	chr13:93279898-93352628	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv983702	chr13:93291025-93353518	Enhancers Weak transcription Active TSS Flanking Active TSS	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	chr13:93307400-93321800	Weak transcription	Right Atrium	heart
2	chr13:93309000-93309800	Enhancers	Fetal Intestine Large	intestine
3	chr13:93309000-93310600	Enhancers	Fetal Intestine Small	intestine

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