Variant report

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10763612	0.84[EUR][1000 genomes]
rs10826316	0.94[ASN][1000 genomes]
rs10826318	0.94[ASN][1000 genomes]
rs10826319	0.94[ASN][1000 genomes]
rs11006582	0.94[ASN][1000 genomes]
rs11006583	0.93[ASN][1000 genomes]
rs11006584	0.94[ASN][1000 genomes]
rs11592742	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11813512	0.98[ASN][1000 genomes]
rs12243790	0.94[ASN][1000 genomes]
rs12254257	0.98[ASN][1000 genomes]
rs12412394	0.94[ASN][1000 genomes]
rs12415285	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12416685	0.98[ASN][1000 genomes]
rs16913790	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1909632	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1909646	0.92[ASN][1000 genomes]
rs2126773	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4301738	0.94[ASN][1000 genomes]
rs4512773	0.94[ASN][1000 genomes]
rs4536156	0.94[ASN][1000 genomes]
rs61860789	0.92[ASN][1000 genomes]
rs61860790	0.92[ASN][1000 genomes]
rs61860852	0.94[ASN][1000 genomes]
rs61860853	0.94[ASN][1000 genomes]
rs7071234	0.94[ASN][1000 genomes]
rs7087374	0.94[ASN][1000 genomes]
rs7087516	0.94[ASN][1000 genomes]
rs72808409	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7919650	0.92[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	nsv895565	chr10:61347537-61379398	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv895566	chr10:61350192-61379398	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv437684	chr10:61354446-61367720	Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv437683	chr10:61354446-61369980	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv1049492	chr10:61357609-61368880	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:61355600-61366800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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