Variant report

Variant	esv3325541
Chromosome Location	chr2:36410473-36413321
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 169 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:169 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199976563	chr2:36410491-36410492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540629385	chr2:36410492-36410493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147259121	chr2:36410500-36410501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs111215042	chr2:36410515-36410516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201599122	chr2:36410530-36410531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs200977679	chr2:36410532-36410533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs9679475	chr2:36410537-36410538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190475746	chr2:36410538-36410539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183690523	chr2:36410562-36410563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs9679476	chr2:36410564-36410565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374242068	chr2:36410596-36410597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201810054	chr2:36410628-36410629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs111154320	chr2:36410658-36410659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs62640431	chr2:36410692-36410693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372091728	chr2:36410788-36410789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373832271	chr2:36410820-36410821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs367724971	chr2:36410852-36410853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs111154321	chr2:36410986-36410987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201118550	chr2:36411074-36411075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs13032057	chr2:36411076-36411077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs111214802	chr2:36411091-36411092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs62651697	chr2:36411106-36411107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs111214760	chr2:36411123-36411124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs111162013	chr2:36411138-36411139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs62651698	chr2:36411140-36411141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371829482	chr2:36411170-36411171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs62651699	chr2:36411172-36411173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201535445	chr2:36411202-36411203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs62651700	chr2:36411204-36411205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370230384	chr2:36411219-36411220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs199536377	chr2:36411234-36411235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs62651701	chr2:36411236-36411237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs111214591	chr2:36411251-36411252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200798759	chr2:36411268-36411269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372147282	chr2:36411276-36411277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562968503	chr2:36411285-36411286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147059098	chr2:36411289-36411290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs111214755	chr2:36411300-36411301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs62651702	chr2:36411305-36411306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548509746	chr2:36411306-36411307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187967130	chr2:36411318-36411319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564057280	chr2:36411320-36411321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs13032545	chr2:36411324-36411325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs377005549	chr2:36411327-36411328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369436323	chr2:36411328-36411329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150132289	chr2:36411349-36411350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200408549	chr2:36411358-36411359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376375214	chr2:36411360-36411361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs13032572	chr2:36411365-36411366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372420210	chr2:36411381-36411382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
T-cell prolymphocytic leukemia	19278963	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
Autism	22495311	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	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	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
Autism	22495309	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:36406400-36413800	Weak transcription	Gastric	stomach

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