Variant report

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

rs_ID	r²[population]
rs55683670	0.86[EUR][1000 genomes]
rs55889336	0.86[EUR][1000 genomes]
rs56089411	0.93[EUR][1000 genomes]
rs56137763	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56327984	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57858513	0.86[EUR][1000 genomes]
rs66504658	0.86[EUR][1000 genomes]
rs66897185	0.86[EUR][1000 genomes]
rs67222609	0.86[EUR][1000 genomes]
rs67283227	0.86[EUR][1000 genomes]
rs67493321	0.80[EUR][1000 genomes]
rs67655085	0.86[EUR][1000 genomes]
rs67856059	0.86[EUR][1000 genomes]
rs67992943	0.80[EUR][1000 genomes]
rs72779018	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72779026	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72779033	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72779034	0.93[EUR][1000 genomes]
rs72779039	0.80[EUR][1000 genomes]
rs72779042	0.86[EUR][1000 genomes]
rs72779049	0.86[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	esv2763469	chr5:91759081-91812497	Enhancers ZNF genes & repeats Weak transcription 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	chr5:91803400-91804000	Enhancers	HUES64 Cell Line	embryonic stem cell

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