Variant report

Variant	rs58364899
Chromosome Location	chr3:86337172-86337173
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1581117	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs57787265	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58704257	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs59095544	0.91[AMR][1000 genomes]
rs59557840	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs59919655	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61641191	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72920670	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72920690	0.91[AMR][1000 genomes]
rs7613658	0.91[AMR][1000 genomes];1.00[EUR][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	nsv532629	chr3:85763873-86608579	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv877115	chr3:86278951-86554319	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 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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