Variant report

Variant	nsv822208
Chromosome Location	chr3:102743602-102752706
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 122 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:122 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs180887871	chr3:102743604-102743605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs545620350	chr3:102743605-102743606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571674828	chr3:102743606-102743607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373489617	chr3:102743607-102743608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557624731	chr3:102743628-102743629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569398020	chr3:102743641-102743642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150748984	chr3:102743662-102743663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544905041	chr3:102743724-102743725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs79296662	chr3:102743769-102743770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539571103	chr3:102743887-102743888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139138467	chr3:102743902-102743903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551805333	chr3:102743947-102743948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545027055	chr3:102743964-102743965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560154159	chr3:102743967-102743968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs142591136	chr3:102743968-102743969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185889513	chr3:102743970-102743971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs192030765	chr3:102743985-102743986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566759271	chr3:102743990-102743991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531414660	chr3:102744010-102744011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs75198967	chr3:102744018-102744019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146029721	chr3:102744019-102744020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs139993148	chr3:102744022-102744023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143495872	chr3:102744050-102744051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566904245	chr3:102744055-102744056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534014871	chr3:102744066-102744067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183262097	chr3:102744164-102744165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377612254	chr3:102744181-102744182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs115673243	chr3:102744260-102744261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538463371	chr3:102744302-102744303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs199873494	chr3:102744308-102744309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145680712	chr3:102744355-102744356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs578252892	chr3:102744378-102744379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187831915	chr3:102744402-102744403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112473562	chr3:102744412-102744413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190746030	chr3:102744421-102744422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572039773	chr3:102744488-102744489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs61525922	chr3:102744505-102744506	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs561059311	chr3:102744523-102744524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531356427	chr3:102744556-102744557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543222046	chr3:102744572-102744573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564778010	chr3:102744574-102744575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532269977	chr3:102744585-102744586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569199309	chr3:102744618-102744619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs547740800	chr3:102744619-102744620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs148514058	chr3:102744629-102744630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs369321516	chr3:102744639-102744640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566736962	chr3:102744656-102744657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs527700649	chr3:102744690-102744691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs549182060	chr3:102744722-102744723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs567765834	chr3:102744772-102744773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:102743200-102745000	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr3:102744600-102746800	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr3:102745000-102746600	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr3:102746000-102746600	Enhancers	iPS-20b Cell Line	embryonic stem cell

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