Variant report

Variant	rs9835765
Chromosome Location	chr3:178751193-178751194
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs11711320	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1542	0.83[ASN][1000 genomes]
rs4245914	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4279147	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4377525	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4395442	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4417911	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4425305	0.88[ASN][1000 genomes]
rs4469018	0.97[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4552405	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4579062	0.97[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4607155	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4632588	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4637331	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4955807	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4955810	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56115013	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6443614	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6443617	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6443618	0.84[AMR][1000 genomes]
rs6772028	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6784495	0.84[AMR][1000 genomes]
rs6790867	0.97[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6793769	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6793893	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6794165	0.86[AMR][1000 genomes]
rs6794956	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6795238	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6800015	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7612363	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7639391	0.97[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9830482	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9831543	0.83[ASN][1000 genomes]
rs9835752	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9846511	0.83[AMR][1000 genomes]
rs9860318	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9860749	0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9878734	0.97[ASN][1000 genomes]
rs9880749	0.97[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998253	chr3:178622707-179196274	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	nsv536814	chr3:178622707-179196274	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	nsv461026	chr3:178661814-178886609	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv592649	chr3:178661814-178886609	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv1009143	chr3:178731525-178783915	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
6	esv1799481	chr3:178733212-178782021	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
7	esv1792927	chr3:178734558-178877169	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
8	esv1841799	chr3:178739594-178884337	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:178716400-178755000	Weak transcription	Pancreas	Pancrea
2	chr3:178722200-178751600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr3:178723800-178754200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr3:178733400-178751400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr3:178733800-178754600	Weak transcription	Lung	lung
6	chr3:178734000-178755200	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr3:178734000-178755400	Weak transcription	HepG2	liver
8	chr3:178735000-178763800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr3:178735800-178751600	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr3:178738000-178764000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr3:178738200-178751600	Weak transcription	Stomach Mucosa	stomach
12	chr3:178738600-178751600	Weak transcription	Adipose Nuclei	Adipose
13	chr3:178738600-178751600	Weak transcription	Gastric	stomach
14	chr3:178738600-178751600	Weak transcription	Ovary	ovary
15	chr3:178738600-178754800	Weak transcription	Spleen	Spleen
16	chr3:178738600-178755000	Weak transcription	Aorta	Aorta
17	chr3:178738600-178757000	Weak transcription	Fetal Stomach	stomach
18	chr3:178738800-178754400	Weak transcription	Psoas Muscle	Psoas
19	chr3:178738800-178755800	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr3:178738800-178757000	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr3:178739400-178751400	Weak transcription	Colon Smooth Muscle	Colon
22	chr3:178739600-178755800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr3:178739800-178754200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr3:178743000-178754600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr3:178743200-178754800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr3:178745400-178754800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr3:178745400-178755600	Weak transcription	NHLF	lung
28	chr3:178745600-178753800	Weak transcription	Fetal Muscle Leg	muscle
29	chr3:178745600-178754400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr3:178745600-178755000	Weak transcription	Left Ventricle	heart
31	chr3:178745600-178758400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr3:178745600-178771800	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr3:178745800-178754200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr3:178745800-178754200	Weak transcription	NHDF-Ad	bronchial
35	chr3:178745800-178755200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr3:178746000-178751400	Weak transcription	HSMMtube	muscle
37	chr3:178746000-178753600	Weak transcription	NH-A	brain
38	chr3:178746000-178756400	Weak transcription	Primary B cells from peripheral blood	blood
39	chr3:178746000-178784000	Weak transcription	Liver	Liver
40	chr3:178746000-178785200	Weak transcription	Thymus	Thymus
41	chr3:178746400-178751600	Weak transcription	Primary hematopoietic stem cells	blood
42	chr3:178746400-178751600	Weak transcription	Brain Hippocampus Middle	brain
43	chr3:178746400-178754000	Weak transcription	NHEK	skin
44	chr3:178746400-178755000	Weak transcription	Brain Anterior Caudate	brain
45	chr3:178746400-178755000	Weak transcription	Brain Cingulate Gyrus	brain
46	chr3:178746600-178751400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr3:178746600-178751400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr3:178746600-178751400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr3:178746600-178751400	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr3:178746600-178751400	Weak transcription	K562	blood

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