Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11948380	0.96[EUR][1000 genomes]
rs11953269	0.91[EUR][1000 genomes]
rs16899990	0.96[EUR][1000 genomes]
rs28870420	0.95[EUR][1000 genomes]
rs4282330	0.90[EUR][1000 genomes]
rs4337863	0.95[EUR][1000 genomes]
rs4343853	0.95[EUR][1000 genomes]
rs4386744	0.96[EUR][1000 genomes]
rs4605801	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs55913729	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs57503003	0.90[EUR][1000 genomes]
rs58624784	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs59615654	0.90[EUR][1000 genomes]
rs6872827	0.96[EUR][1000 genomes]
rs73084983	0.95[EUR][1000 genomes]
rs73754648	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73754668	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73755029	0.84[AMR][1000 genomes]
rs7733219	0.96[EUR][1000 genomes]
rs7733353	0.95[EUR][1000 genomes]
rs7735950	0.95[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	nsv881635	chr5:30122190-30371238	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:30142600-30143200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:30142600-30143400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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