Variant report

Variant	nsv980141
Chromosome Location	chr4:91313793-91315379
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:60 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191532380	chr4:91313800-91313801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs386677179	chr4:91313830-91313831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182290109	chr4:91313832-91313833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188142717	chr4:91313843-91313844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs115699137	chr4:91313930-91313931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567718813	chr4:91313945-91313946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs370207119	chr4:91313993-91313994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192834735	chr4:91313994-91313995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs76791680	chr4:91314007-91314008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554790185	chr4:91314058-91314059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs111657979	chr4:91314067-91314068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190142351	chr4:91314179-91314180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558963518	chr4:91314211-91314212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192575358	chr4:91314288-91314289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs546217182	chr4:91314292-91314293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539813600	chr4:91314297-91314298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374353409	chr4:91314327-91314328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559825101	chr4:91314365-91314366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573356497	chr4:91314375-91314376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs13104743	chr4:91314397-91314398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs13104752	chr4:91314413-91314414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564580287	chr4:91314495-91314496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184828807	chr4:91314560-91314561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368379425	chr4:91314586-91314587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562384807	chr4:91314614-91314615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146105714	chr4:91314635-91314636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574547954	chr4:91314651-91314652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540437550	chr4:91314667-91314668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551673948	chr4:91314670-91314671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189246907	chr4:91314690-91314691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs73832781	chr4:91314706-91314707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112882643	chr4:91314710-91314711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532565262	chr4:91314780-91314781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191204855	chr4:91314792-91314793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs180988766	chr4:91314904-91314905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200070904	chr4:91314929-91314930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201100366	chr4:91314944-91314945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35646666	chr4:91314945-91314946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536782852	chr4:91314949-91314950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546121185	chr4:91315019-91315020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550283421	chr4:91315023-91315024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs116796591	chr4:91315026-91315027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs7660558	chr4:91315035-91315036	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs114778381	chr4:91315043-91315044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572612143	chr4:91315053-91315054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12331262	chr4:91315060-91315061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528025023	chr4:91315097-91315098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561898306	chr4:91315117-91315118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536687735	chr4:91315124-91315125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185913655	chr4:91315173-91315174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Acute monocytic leukemia	16498392	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Obesity	20622171	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:91296400-91325000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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