Variant report

Variant	rs6792895
Chromosome Location	chr3:109317142-109317143
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs16855810	1.00[AMR][1000 genomes]
rs58862465	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60563567	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs6437861	1.00[AMR][1000 genomes]
rs6793082	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7340726	0.90[AMR][1000 genomes]
rs73850998	1.00[AMR][1000 genomes]
rs73850999	0.89[AMR][1000 genomes]
rs73851000	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73851001	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7618622	1.00[AMR][1000 genomes]
rs7652437	1.00[AMR][1000 genomes]
rs7652626	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460814	chr3:109195046-109381428	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
2	nsv591268	chr3:109195046-109381428	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
3	nsv470827	chr3:109195046-109433855	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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