Variant report

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs11119653	0.82[AFR][1000 genomes]
rs11119665	1.00[EUR][1000 genomes]
rs12061710	1.00[EUR][1000 genomes]
rs12063183	1.00[EUR][1000 genomes]
rs12063554	1.00[EUR][1000 genomes]
rs12064954	1.00[EUR][1000 genomes]
rs12065047	1.00[EUR][1000 genomes]
rs12067778	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12070528	1.00[EUR][1000 genomes]
rs12076586	1.00[EUR][1000 genomes]
rs12078498	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12079934	1.00[EUR][1000 genomes]
rs12084637	1.00[EUR][1000 genomes]
rs12086827	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12089911	1.00[EUR][1000 genomes]
rs17017024	1.00[EUR][1000 genomes]
rs57654955	1.00[EUR][1000 genomes]
rs73071568	1.00[EUR][1000 genomes]
rs73071587	1.00[EUR][1000 genomes]
rs73073478	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73073488	1.00[EUR][1000 genomes]
rs73075420	1.00[EUR][1000 genomes]
rs73075431	1.00[EUR][1000 genomes]
rs73075455	1.00[EUR][1000 genomes]
rs73075457	1.00[EUR][1000 genomes]
rs73075496	1.00[EUR][1000 genomes]
rs7547391	1.00[EUR][1000 genomes]
rs7554031	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][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	nsv524740	chr1:211143108-211155614	Enhancers Strong transcription Weak transcription	n/a	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	chr1:211123000-211152000	Weak transcription	HSMM	muscle

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