Variant report

Variant	nsv528401
Chromosome Location	chr2:56706758-56712426
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189993992	chr2:56710012-56710013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs542883066	chr2:56710013-56710014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs549649854	chr2:56710015-56710016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181502500	chr2:56710039-56710040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs186171626	chr2:56710079-56710080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs550186831	chr2:56710121-56710122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551375720	chr2:56710128-56710129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569479972	chr2:56710149-56710150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190837024	chr2:56710153-56710154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538398602	chr2:56710160-56710161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547182411	chr2:56710165-56710166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs6738570	chr2:56710188-56710189	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs138732504	chr2:56710192-56710193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538622177	chr2:56710234-56710235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs549617876	chr2:56710264-56710265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576849870	chr2:56710365-56710366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs6753780	chr2:56710407-56710408	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs557722540	chr2:56710428-56710429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs547101773	chr2:56710432-56710433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs577626534	chr2:56710449-56710450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534252806	chr2:56710460-56710461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181944921	chr2:56710474-56710475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs573748426	chr2:56710486-56710487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149341304	chr2:56710536-56710537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567001510	chr2:56710550-56710551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562703754	chr2:56710558-56710559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs576399273	chr2:56710559-56710560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545360279	chr2:56710573-56710574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564825274	chr2:56710585-56710586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs527289249	chr2:56710586-56710587	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
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
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	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
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Mental retardation	19951919	CNVD
Myelofibrosis	22110671	CNVD
Microcephaly	20799320	CNVD
camptodactyly	20799320	CNVD
cognitive delay	20799320	CNVD
prenatal and postnatal growth deficiency	20799320	CNVD
ptosis of eyelids	20799320	CNVD
Maculopathy	20981449	CNVD
2p16.1 microdeletion syndrome	22283845	CNVD
Autism	22579565	CNVD
Autism	16963482	CNVD
Autism	21750575	CNVD
idiopathic intellectual disability	16963482	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Multiple myeloma	16616336	CNVD
Follicular lymphoma	17699855	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:56710000-56710600	Enhancers	Muscle Satellite Cultured Cells	--
2	chr2:56710000-56710600	Enhancers	HSMM	muscle

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