Variant report

Variant	rs62528836
Chromosome Location	chr9:8781162-8781163
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:30)

rs_ID	r²[population]
rs10116829	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1036329	0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10511509	0.83[EUR][1000 genomes]
rs10815942	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10815943	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10815944	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10977289	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10977295	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10977296	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10977298	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12337561	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12343337	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12350351	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1549998	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1549999	0.81[EUR][1000 genomes]
rs17576912	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17660536	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17660571	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4606116	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62528808	0.85[ASN][1000 genomes]
rs62528809	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs62528810	0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs62528832	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62528833	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62528834	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62528835	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62528837	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62528838	0.95[ASN][1000 genomes]
rs9299073	0.83[EUR][1000 genomes]
rs9299074	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	nsv892235	chr9:8700396-8865925	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1025800	chr9:8712487-9030627	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv539980	chr9:8712487-9030627	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv892236	chr9:8745520-8870553	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv892237	chr9:8752743-8794314	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	inside rSNPs	diseases
7	nsv1015898	chr9:8753534-9011443	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv892238	chr9:8757828-8794314	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	inside rSNPs	diseases
9	nsv892239	chr9:8773599-8805462	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region	1 gene(s)	inside rSNPs	diseases
10	esv2761247	chr9:8775019-8786718	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8764800-8783600	Weak transcription	Fetal Stomach	stomach
2	chr9:8777600-8782000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr9:8778000-8781200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr9:8778000-8782000	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr9:8778200-8781400	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr9:8778200-8781600	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr9:8778400-8781800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr9:8778400-8782000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr9:8778600-8781600	Weak transcription	Ovary	ovary
10	chr9:8778600-8785600	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr9:8778800-8798600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr9:8779000-8781200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr9:8779000-8781800	Enhancers	Brain Anterior Caudate	brain
14	chr9:8779000-8782000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr9:8779200-8781800	Enhancers	Brain Hippocampus Middle	brain
16	chr9:8779600-8781800	Enhancers	Brain Angular Gyrus	brain
17	chr9:8779600-8781800	Enhancers	Fetal Lung	lung
18	chr9:8779800-8781400	Enhancers	Brain Substantia Nigra	brain
19	chr9:8779800-8781600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr9:8779800-8784000	Weak transcription	Aorta	Aorta
21	chr9:8779800-8784600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr9:8780000-8782000	Enhancers	Brain Cingulate Gyrus	brain
23	chr9:8780200-8781200	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr9:8780400-8781200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr9:8780600-8781800	Enhancers	Fetal Kidney	kidney
26	chr9:8780800-8781200	Weak transcription	Fetal Heart	heart
27	chr9:8780800-8782000	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr9:8780800-8782000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr9:8781000-8781600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr9:8781000-8781600	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr9:8781000-8781800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr9:8781000-8782000	Enhancers	Liver	Liver

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