Variant report

Variant	rs4417561
Chromosome Location	chr16:80011359-80011360
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]
rs34302186	0.86[EUR][1000 genomes]
rs4146391	0.96[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs4243196	0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4438317	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4603572	0.84[EUR][1000 genomes]
rs5029361	0.96[EUR][1000 genomes]
rs61336918	0.96[EUR][1000 genomes]
rs7192512	0.85[EUR][1000 genomes]
rs8051754	0.84[EUR][1000 genomes]
rs9929751	0.83[AFR][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	nsv573285	chr16:79158182-80127326	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv573294	chr16:80005642-80131944	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:80006400-80015000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr16:80008400-80011800	Weak transcription	K562	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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