Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs56079800	0.90[AFR][1000 genomes]
rs56275714	1.00[EUR][1000 genomes]
rs58052452	0.90[AFR][1000 genomes]
rs59351555	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59598125	1.00[AMR][1000 genomes]
rs59802548	0.90[AFR][1000 genomes]
rs60410633	1.00[AMR][1000 genomes]
rs73771636	0.90[AFR][1000 genomes]
rs73771637	0.90[AFR][1000 genomes]
rs73771638	0.90[AFR][1000 genomes]
rs73771640	0.80[AFR][1000 genomes]
rs73771642	0.90[AFR][1000 genomes]
rs73771643	0.90[AFR][1000 genomes]
rs73771646	0.90[AFR][1000 genomes]
rs73772083	0.80[AFR][1000 genomes]
rs73772084	0.80[AFR][1000 genomes]
rs73772085	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73772457	0.81[AFR][1000 genomes]
rs73772458	0.90[AFR][1000 genomes]
rs73772461	0.90[AFR][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	esv1001926	chr5:68281457-68292160	Enhancers Flanking Active TSS Weak transcription	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	chr5:68282800-68283200	Enhancers	HUES64 Cell Line	embryonic stem cell

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