Variant report

Variant	rs9802651
Chromosome Location	chr9:16235907-16235908
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12002237	0.93[ASN][1000 genomes]
rs12003973	0.93[ASN][1000 genomes]
rs12003991	0.93[ASN][1000 genomes]
rs16934286	0.83[ASN][1000 genomes]
rs16934287	0.83[ASN][1000 genomes]
rs4961468	0.81[ASN][1000 genomes]
rs4961469	0.83[ASN][1000 genomes]
rs4961471	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4961674	0.92[EUR][1000 genomes]
rs4961675	0.92[EUR][1000 genomes]
rs4961676	0.94[EUR][1000 genomes]
rs4961678	0.81[ASN][1000 genomes]
rs4961679	0.83[ASN][1000 genomes]
rs4961680	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4961681	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4961683	0.92[ASN][1000 genomes]
rs56119294	0.83[ASN][1000 genomes]
rs57847950	0.83[ASN][1000 genomes]
rs59560725	0.93[ASN][1000 genomes]
rs73425617	0.92[EUR][1000 genomes]
rs73425648	0.93[ASN][1000 genomes]
rs9407728	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9407729	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9407730	0.83[ASN][1000 genomes]
rs9407732	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9802678	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949463	chr9:15970668-16377360	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv429999	chr9:16102066-16389100	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv892639	chr9:16190403-16242088	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv892640	chr9:16206695-16260837	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv892641	chr9:16218659-16242088	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv892642	chr9:16233085-16282979	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16232800-16236000	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr9:16235000-16236000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:16235200-16243200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr9:16235400-16237600	Enhancers	Fetal Lung	lung
5	chr9:16235400-16242400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr9:16235600-16236600	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr9:16235600-16236600	Enhancers	Fetal Stomach	stomach
8	chr9:16235800-16236000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
9	chr9:16235800-16236800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr9:16235800-16237400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr9:16235800-16237400	Enhancers	NHLF	lung
12	chr9:16235800-16239000	Enhancers	NHDF-Ad	bronchial
13	chr9:16235800-16239200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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