Variant report

Variant	rs12347322
Chromosome Location	chr9:26659279-26659280
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10118730	1.00[EUR][1000 genomes]
rs10118861	1.00[EUR][1000 genomes]
rs10120824	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10124005	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10125924	1.00[EUR][1000 genomes]
rs1117679	1.00[EUR][1000 genomes]
rs1117680	1.00[EUR][1000 genomes]
rs12336769	1.00[EUR][1000 genomes]
rs12337751	1.00[EUR][1000 genomes]
rs12339885	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12344232	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16910504	1.00[EUR][1000 genomes]
rs1812846	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28451412	1.00[EUR][1000 genomes]
rs28816460	1.00[EUR][1000 genomes]
rs73429823	1.00[EUR][1000 genomes]
rs73429839	1.00[EUR][1000 genomes]
rs73429855	1.00[EUR][1000 genomes]
rs73429860	1.00[EUR][1000 genomes]
rs73429861	1.00[EUR][1000 genomes]
rs73429862	1.00[EUR][1000 genomes]
rs73429863	1.00[EUR][1000 genomes]
rs73429867	1.00[EUR][1000 genomes]
rs73429871	1.00[EUR][1000 genomes]
rs73429872	1.00[EUR][1000 genomes]
rs73429880	1.00[EUR][1000 genomes]
rs7854682	1.00[EUR][1000 genomes]
rs7856088	1.00[EUR][1000 genomes]
rs7863872	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv995049	chr9:26162115-26760535	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv892854	chr9:26326100-26749094	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1022674	chr9:26453723-26668102	Enhancers Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1020439	chr9:26453723-26669855	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1022289	chr9:26453723-26670583	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv892858	chr9:26609613-26783463	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv466330	chr9:26641557-26691668	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	lncRNA	n/a	inside rSNPs	diseases
8	nsv613939	chr9:26641557-26691668	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	lncRNA	n/a	inside rSNPs	diseases
9	nsv466331	chr9:26643035-26689442	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	lncRNA	n/a	inside rSNPs	diseases
10	nsv613940	chr9:26643035-26689442	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	lncRNA	n/a	inside rSNPs	diseases
11	nsv892859	chr9:26643035-26691668	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer	lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:26656200-26659600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr9:26657600-26659600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr9:26658200-26659400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr9:26659000-26659600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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