Variant report

Variant	nsv581516
Chromosome Location	chr2:40931058-40940311
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:56 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181697039	chr2:40939220-40939221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs4101520	chr2:40939221-40939222	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs186145357	chr2:40939280-40939281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566469342	chr2:40939291-40939292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189344407	chr2:40939318-40939319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs527345677	chr2:40939319-40939320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs181927892	chr2:40939321-40939322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571879116	chr2:40939392-40939393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs7598736	chr2:40939457-40939458	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs557607751	chr2:40939463-40939464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569437261	chr2:40939465-40939466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536753339	chr2:40939492-40939493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554718494	chr2:40939535-40939536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs374540851	chr2:40939545-40939546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs144578807	chr2:40939580-40939581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs570785244	chr2:40939620-40939621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs116592666	chr2:40939624-40939625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs367793885	chr2:40939627-40939628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs576751143	chr2:40939629-40939630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544067703	chr2:40939664-40939665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562353272	chr2:40939680-40939681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs371206077	chr2:40939707-40939708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537581182	chr2:40939713-40939714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs185913913	chr2:40939728-40939729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541624973	chr2:40939738-40939739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs560032815	chr2:40939746-40939747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs527366818	chr2:40939758-40939759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs551911665	chr2:40939782-40939783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190940220	chr2:40939793-40939794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556218288	chr2:40939820-40939821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs532868702	chr2:40939952-40939953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs577787316	chr2:40939984-40939985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551252881	chr2:40940007-40940008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112794615	chr2:40940015-40940016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553973193	chr2:40940060-40940061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369084996	chr2:40940067-40940068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141617123	chr2:40940105-40940106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs77987294	chr2:40940122-40940123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534272141	chr2:40940126-40940127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567533690	chr2:40940146-40940147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558696698	chr2:40940148-40940149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183259451	chr2:40940171-40940172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544105796	chr2:40940180-40940181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556088940	chr2:40940195-40940196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574385172	chr2:40940211-40940212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541695165	chr2:40940212-40940213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186477644	chr2:40940235-40940236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs13017035	chr2:40940248-40940249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572066888	chr2:40940257-40940258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191776897	chr2:40940266-40940267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40939200-40939800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr2:40939200-40939800	Enhancers	HSMMtube	muscle
3	chr2:40939400-40940000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr2:40940000-40944200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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