Variant report

Variant	rs3763653
Chromosome Location	chr9:8518395-8518396
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10117042	0.83[CHD][hapmap];0.83[JPT][hapmap];0.91[MEX][hapmap];0.89[ASN][1000 genomes]
rs10120190	0.93[CEU][hapmap];0.91[CHD][hapmap];0.81[GIH][hapmap];0.83[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10123125	0.85[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.94[ASN][1000 genomes]
rs10123138	0.85[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10124867	0.82[JPT][hapmap];0.88[ASN][1000 genomes]
rs10511499	0.93[CHB][hapmap];0.82[CHD][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.97[ASN][1000 genomes]
rs10758978	0.96[ASN][1000 genomes]
rs10758979	0.85[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.81[TSI][hapmap];0.95[ASN][1000 genomes]
rs10758980	0.85[CEU][hapmap];0.93[CHB][hapmap];0.83[JPT][hapmap];0.94[ASN][1000 genomes]
rs10815883	0.86[CHB][hapmap];0.83[JPT][hapmap]
rs10815896	0.92[JPT][hapmap];0.89[ASN][1000 genomes]
rs10815898	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10815900	0.86[GIH][hapmap];0.81[TSI][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10815905	0.92[ASN][1000 genomes]
rs10815906	0.85[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.81[TSI][hapmap];0.95[ASN][1000 genomes]
rs10815907	0.85[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10815908	0.93[CHB][hapmap];0.83[JPT][hapmap];0.95[ASN][1000 genomes]
rs10977146	0.83[JPT][hapmap]
rs10977169	0.89[CEU][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10977170	0.91[CEU][hapmap];0.89[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10977181	0.85[CEU][hapmap];0.80[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10977189	0.91[ASN][1000 genomes]
rs10977192	0.82[ASN][1000 genomes]
rs12340211	0.93[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs12341045	0.86[ASN][1000 genomes]
rs12341078	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs12344975	0.85[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs12683581	0.83[JPT][hapmap]
rs12686431	0.83[JPT][hapmap]
rs17650044	0.83[JPT][hapmap]
rs1998513	0.85[CHD][hapmap];0.91[GIH][hapmap];0.83[JPT][hapmap];0.86[ASN][1000 genomes]
rs1998515	0.85[CHB][hapmap];0.87[ASN][1000 genomes]
rs2273998	0.86[CHB][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.85[TSI][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3763652	0.93[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6477313	0.86[CHB][hapmap];0.83[JPT][hapmap];0.86[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	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	nsv892226	chr9:8435525-8522326	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	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
5	nsv892229	chr9:8485201-8520366	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	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

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8420600-8557600	Weak transcription	Aorta	Aorta
2	chr9:8442200-8522200	Weak transcription	Liver	Liver
3	chr9:8483800-8524800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr9:8486000-8519400	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr9:8486000-8522200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr9:8486200-8522800	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr9:8486200-8523200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr9:8486200-8531600	Weak transcription	Fetal Kidney	kidney
9	chr9:8487000-8521200	Weak transcription	Brain Germinal Matrix	brain
10	chr9:8487000-8521200	Weak transcription	Dnd41	blood
11	chr9:8492400-8528800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr9:8493000-8521200	Weak transcription	Fetal Muscle Leg	muscle
13	chr9:8493200-8523200	Weak transcription	Fetal Stomach	stomach
14	chr9:8493200-8531200	Weak transcription	Fetal Brain Female	brain
15	chr9:8494200-8531200	Weak transcription	Fetal Brain Male	brain
16	chr9:8495600-8520400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr9:8509400-8528600	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr9:8509600-8521200	Weak transcription	Brain Hippocampus Middle	brain
19	chr9:8509800-8521200	Weak transcription	Brain Substantia Nigra	brain
20	chr9:8509800-8532800	Weak transcription	Brain Angular Gyrus	brain
21	chr9:8510000-8521200	Weak transcription	Brain Anterior Caudate	brain
22	chr9:8513200-8523000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr9:8513600-8521200	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr9:8517000-8522400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr9:8517000-8523600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr9:8517200-8518400	Strong transcription	Fetal Lung	lung
27	chr9:8517200-8518400	Strong transcription	Fetal Muscle Trunk	muscle
28	chr9:8517600-8518400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr9:8517600-8518400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr9:8517600-8518400	Strong transcription	Primary hematopoietic stem cells	blood
31	chr9:8517800-8518400	Strong transcription	Ovary	ovary
32	chr9:8518000-8528600	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr9:8518200-8519400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr9:8518200-8526400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links