Variant report

Variant	rs1323582
Chromosome Location	chr9:8559267-8559268
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10977204	0.95[EUR][1000 genomes]
rs10977209	0.82[EUR][1000 genomes]
rs12004302	0.87[CEU][hapmap];0.84[EUR][1000 genomes]
rs12004691	0.93[EUR][1000 genomes]
rs12006485	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16928124	0.87[CEU][hapmap];0.94[CHB][hapmap];0.86[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs55785812	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs58733780	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs58948334	0.83[EUR][1000 genomes]
rs61027185	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73430464	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs73640929	0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs73640931	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7854007	0.94[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031472	chr9:8250901-8712547	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv1022796	chr9:8360729-9110046	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv892228	chr9:8482778-8703733	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv831504	chr9:8496277-8665773	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv1026208	chr9:8534915-8595338	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8534600-8564000	Weak transcription	Primary hematopoietic stem cells	blood
2	chr9:8553000-8561400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr9:8553600-8571000	Weak transcription	Brain Anterior Caudate	brain
4	chr9:8553800-8559400	Weak transcription	Brain Angular Gyrus	brain
5	chr9:8556000-8560600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr9:8556000-8561200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr9:8556200-8559400	Weak transcription	Brain Hippocampus Middle	brain
8	chr9:8556200-8559600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr9:8556200-8560800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr9:8556200-8571200	Weak transcription	Ovary	ovary
11	chr9:8556400-8568200	Weak transcription	Brain Substantia Nigra	brain
12	chr9:8556600-8570600	Weak transcription	Fetal Lung	lung
13	chr9:8557200-8561000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr9:8557200-8561400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr9:8557400-8575200	Weak transcription	Fetal Kidney	kidney
16	chr9:8558600-8559600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr9:8558600-8559800	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr9:8558600-8571000	Weak transcription	Pancreas	Pancrea
19	chr9:8559000-8564200	Weak transcription	Fetal Stomach	stomach
20	chr9:8559200-8559800	Enhancers	Brain Inferior Temporal Lobe	brain

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