Variant report

Variant	rs6994952
Chromosome Location	chr8:64566513-64566514
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1520920	1.00[EUR][1000 genomes]
rs57448152	1.00[EUR][1000 genomes]
rs705981	1.00[EUR][1000 genomes]
rs73269072	1.00[AMR][1000 genomes]
rs73269080	1.00[AMR][1000 genomes]
rs73270941	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73270950	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73270961	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7819256	1.00[EUR][1000 genomes]
rs7830446	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	nsv831343	chr8:64436268-64642328	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:64561000-64569200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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