Variant report

Variant	rs327713
Chromosome Location	chr7:80837066-80837067
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs172911	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs179174	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs182752	0.83[AMR][1000 genomes]
rs325969	0.80[AFR][1000 genomes]
rs325981	0.91[YRI][hapmap]
rs325982	0.91[YRI][hapmap]
rs327628	0.83[AMR][1000 genomes]
rs327629	0.83[AMR][1000 genomes]
rs327641	0.83[AMR][1000 genomes]
rs327642	0.83[AMR][1000 genomes]
rs327643	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs327645	0.83[AMR][1000 genomes]
rs327646	0.83[AMR][1000 genomes]
rs327648	0.83[AMR][1000 genomes]
rs327714	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs327715	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs327717	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs327721	0.83[AMR][1000 genomes]
rs327722	0.83[AMR][1000 genomes]
rs327740	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs327741	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs327748	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs475840	0.83[AMR][1000 genomes]
rs475847	0.83[AMR][1000 genomes]
rs59506860	0.83[AMR][1000 genomes]
rs74271	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034690	chr7:80520004-80987682	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv831044	chr7:80721773-80918591	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv888557	chr7:80813081-80917148	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1023149	chr7:80817550-80928090	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80835800-80838800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr7:80836000-80837200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:80837000-80837400	Active TSS	K562	blood
4	chr7:80837000-80838000	Weak transcription	NHDF-Ad	bronchial
5	chr7:80837000-80838400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr7:80837000-80839600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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