Variant report

Variant	rs8047520
Chromosome Location	chr16:80002179-80002180
allele	A/C
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:11)

rs_ID	r²[population]
rs16951747	1.00[AMR][1000 genomes]
rs16951756	1.00[AMR][1000 genomes]
rs16951851	1.00[AMR][1000 genomes]
rs16951900	1.00[AMR][1000 genomes]
rs16951905	1.00[AMR][1000 genomes]
rs16951936	1.00[AMR][1000 genomes]
rs4433822	1.00[AMR][1000 genomes]
rs55964243	1.00[AMR][1000 genomes]
rs58463189	1.00[AMR][1000 genomes]
rs8051245	1.00[AMR][1000 genomes]
rs8052968	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 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

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:79997000-80006200	Weak transcription	Right Atrium	heart
2	chr16:80000400-80002200	Weak transcription	K562	blood
3	chr16:80000600-80005800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr16:80000600-80006000	Weak transcription	Primary monocytes fromperipheralblood	blood

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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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