Variant report

Variant	rs73478292
Chromosome Location	chr9:84598897-84598898
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs57951881	1.00[AMR][1000 genomes]
rs73463413	1.00[AMR][1000 genomes]
rs73463420	1.00[AMR][1000 genomes]
rs73463449	1.00[AMR][1000 genomes]
rs73463466	1.00[AMR][1000 genomes]
rs73463470	1.00[AMR][1000 genomes]
rs73463482	1.00[AMR][1000 genomes]
rs73478281	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73480313	1.00[AMR][1000 genomes]
rs73480314	1.00[AMR][1000 genomes]
rs73480317	1.00[AMR][1000 genomes]
rs73480322	1.00[AMR][1000 genomes]
rs73480325	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831639	chr9:84501548-84651151	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv6584	chr9:84547871-84606452	Enhancers ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr9:84596000-84599600	Weak transcription	Adipose Derived Mesenchymal Stem Cell 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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