Variant report

Variant	rs13295668
Chromosome Location	chr9:26689235-26689236
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10967477	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12377464	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12380443	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13284705	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13284937	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13285927	0.81[AMR][1000 genomes]
rs13286139	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13289000	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13289242	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13292094	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13292180	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13292559	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13294589	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13295730	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13295742	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13298607	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1434480	0.80[AMR][1000 genomes]
rs17755083	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35176178	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs36002225	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4531131	0.88[AMR][1000 genomes]
rs67775442	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 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	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
4	nsv466330	chr9:26641557-26691668	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	lncRNA	n/a	inside rSNPs	diseases
5	nsv613939	chr9:26641557-26691668	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	lncRNA	n/a	inside rSNPs	diseases
6	nsv466331	chr9:26643035-26689442	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	lncRNA	n/a	inside rSNPs	diseases
7	nsv613940	chr9:26643035-26689442	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	lncRNA	n/a	inside rSNPs	diseases
8	nsv892859	chr9:26643035-26691668	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer	lncRNA	n/a	inside rSNPs	diseases
9	esv2508182	chr9:26689086-26690489	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:26687800-26694200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:26689200-26689400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr9:26689200-26689400	Enhancers	Cortex derived primary cultured neurospheres	brain

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