Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11119665	1.00[EUR][1000 genomes]
rs12059232	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12061710	1.00[EUR][1000 genomes]
rs12063183	1.00[EUR][1000 genomes]
rs12063554	1.00[EUR][1000 genomes]
rs12064044	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12064954	1.00[EUR][1000 genomes]
rs12065047	1.00[EUR][1000 genomes]
rs12067778	1.00[EUR][1000 genomes]
rs12078498	1.00[EUR][1000 genomes]
rs12086827	1.00[EUR][1000 genomes]
rs12089911	1.00[EUR][1000 genomes]
rs12093116	0.90[AFR][1000 genomes]
rs17017024	1.00[EUR][1000 genomes]
rs57654955	1.00[EUR][1000 genomes]
rs58263592	1.00[EUR][1000 genomes]
rs73071568	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73071583	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73071589	1.00[AMR][1000 genomes]
rs73073478	1.00[EUR][1000 genomes]
rs73073488	1.00[EUR][1000 genomes]
rs73075420	1.00[EUR][1000 genomes]
rs73075431	1.00[EUR][1000 genomes]
rs74156855	1.00[AMR][1000 genomes]
rs7547391	1.00[EUR][1000 genomes]
rs7554031	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832503	chr1:210948760-211103163	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv873154	chr1:211057697-211117197	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	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	chr1:211093400-211110800	Weak transcription	HSMM	muscle

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