Variant report

Variant	rs9823236
Chromosome Location	chr3:81700361-81700362
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs11917955	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11918127	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11922101	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13314509	0.94[YRI][hapmap]
rs13319440	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13320194	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs13433893	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs17019144	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17019176	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2291593	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3772906	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3772907	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3821555	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs55828412	0.81[ASN][1000 genomes]
rs56037559	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57135543	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58104973	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6762839	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6766394	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6774605	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6805400	1.00[CHB][hapmap];0.90[JPT][hapmap];0.95[YRI][hapmap]
rs72904388	0.81[ASN][1000 genomes]
rs72904392	0.81[ASN][1000 genomes]
rs72904402	0.81[ASN][1000 genomes]
rs72906226	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7617859	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7619190	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7629051	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7642141	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs9309873	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9810626	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9811220	0.89[YRI][hapmap]
rs9811796	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs9815184	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9820089	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9823805	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9828883	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9842415	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9842657	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9844254	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.93[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9854689	0.94[YRI][hapmap]
rs9862555	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9865935	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9876575	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9878273	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9879273	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9881652	0.89[YRI][hapmap]
rs998205	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs998207	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933756	chr3:81413060-81754738	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1003217	chr3:81435044-81752521	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1012133	chr3:81499082-81817471	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv933259	chr3:81523854-81730617	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv949545	chr3:81523898-81893929	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv999587	chr3:81534364-81707800	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv536603	chr3:81534364-81707800	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv1009607	chr3:81651419-81825151	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
9	nsv536604	chr3:81651419-81825151	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
10	nsv834749	chr3:81655377-81818880	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
11	nsv999992	chr3:81693662-82015969	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
12	nsv536605	chr3:81693662-82015969	Flanking Active TSS Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
13	nsv963523	chr3:81698115-81702818	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:81603600-81726400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr3:81627400-81755000	Weak transcription	Primary B cells from cord blood	blood
3	chr3:81635000-81700800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr3:81642000-81753000	Weak transcription	HUVEC	blood vessel
5	chr3:81642200-81712200	Weak transcription	Ovary	ovary
6	chr3:81662200-81703000	Weak transcription	HSMMtube	muscle
7	chr3:81678600-81701600	Strong transcription	Dnd41	blood
8	chr3:81680600-81703000	Weak transcription	Hela-S3	cervix
9	chr3:81682400-81706600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr3:81684400-81712400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr3:81687400-81700600	Weak transcription	NH-A	brain
12	chr3:81689000-81712200	Weak transcription	Lung	lung
13	chr3:81689600-81712200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr3:81689600-81726200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr3:81689600-81744000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr3:81689800-81744000	Weak transcription	Right Ventricle	heart
17	chr3:81693000-81700400	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr3:81693000-81726800	Weak transcription	GM12878-XiMat	blood
19	chr3:81693200-81700600	Weak transcription	Primary T cells from cord blood	blood
20	chr3:81694000-81707800	Weak transcription	HepG2	liver
21	chr3:81695200-81748000	Weak transcription	Aorta	Aorta
22	chr3:81695400-81700400	Weak transcription	Fetal Heart	heart
23	chr3:81695400-81733800	Weak transcription	HSMM	muscle
24	chr3:81695400-81746200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr3:81695600-81728400	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr3:81698200-81700400	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr3:81699000-81700400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr3:81699000-81702000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr3:81699200-81700600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr3:81699200-81700800	Enhancers	NHEK	skin
31	chr3:81699200-81701600	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr3:81699200-81704400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr3:81699200-81709600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr3:81699200-81712400	Weak transcription	Adipose Nuclei	Adipose
35	chr3:81699200-81715600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr3:81699200-81717400	Weak transcription	NHDF-Ad	bronchial
37	chr3:81699400-81707400	Weak transcription	Liver	Liver
38	chr3:81699400-81766000	Weak transcription	NHLF	lung
39	chr3:81699600-81700400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr3:81699600-81701400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr3:81699800-81701200	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr3:81699800-81701400	Genic enhancers	Left Ventricle	heart
43	chr3:81700000-81700800	Enhancers	Stomach Mucosa	stomach
44	chr3:81700000-81701400	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr3:81700200-81701000	Weak transcription	Psoas Muscle	Psoas
46	chr3:81700200-81701200	Weak transcription	Esophagus	oesophagus

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