Variant report

Variant	rs9449337
Chromosome Location	chr6:82211572-82211573
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10943814	1.00[AMR][1000 genomes]
rs1419031	1.00[AMR][1000 genomes]
rs6906164	1.00[AMR][1000 genomes]
rs6911333	1.00[AMR][1000 genomes]
rs6914841	1.00[AMR][1000 genomes]
rs73751413	1.00[AMR][1000 genomes]
rs9294227	1.00[AMR][1000 genomes]
rs9443904	1.00[AMR][1000 genomes]
rs9443906	1.00[AMR][1000 genomes]
rs9443917	1.00[AMR][1000 genomes]
rs9443918	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9443932	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9449301	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9449306	1.00[AMR][1000 genomes]
rs9449315	1.00[AMR][1000 genomes]
rs9449317	1.00[AMR][1000 genomes]
rs9449334	1.00[AMR][1000 genomes]
rs9449335	0.89[AFR][1000 genomes];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	nsv604087	chr6:81792413-82326091	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1032655	chr6:81942397-82225830	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 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	chr6:82210000-82212800	Weak transcription	Fetal Heart	heart

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

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