Variant report

Variant	nsv292961
Chromosome Location	chr4:159027378-159028491
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:63 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28973207	chr4:159027378-159027379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs191011137	chr4:159027404-159027405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs578091587	chr4:159027413-159027414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs114582426	chr4:159027420-159027421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs28971583	chr4:159027432-159027433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558499666	chr4:159027445-159027446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183557831	chr4:159027459-159027460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143461501	chr4:159027462-159027463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200761650	chr4:159027474-159027475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370448186	chr4:159027476-159027477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs373069485	chr4:159027481-159027482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs377031533	chr4:159027482-159027483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370989668	chr4:159027485-159027486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187910189	chr4:159027495-159027496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs572902469	chr4:159027502-159027503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544361567	chr4:159027507-159027508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs376612399	chr4:159027568-159027569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs62652515	chr4:159027653-159027654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561458891	chr4:159027776-159027777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376016778	chr4:159027801-159027802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201733975	chr4:159027808-159027809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374336774	chr4:159027830-159027831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200075293	chr4:159027831-159027832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201969026	chr4:159027832-159027833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368187645	chr4:159027833-159027834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201210864	chr4:159027840-159027841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574929136	chr4:159027845-159027846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114874705	chr4:159027863-159027864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201975850	chr4:159027917-159027918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374623636	chr4:159027919-159027920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201509712	chr4:159027925-159027926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374099718	chr4:159027929-159027930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs367993726	chr4:159027930-159027931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371487250	chr4:159027933-159027934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111216315	chr4:159027943-159027944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs199700571	chr4:159027947-159027948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368569270	chr4:159027966-159027967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560678548	chr4:159027967-159027968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372639401	chr4:159027971-159027972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs115420439	chr4:159027975-159027976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111205673	chr4:159027978-159027979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377087335	chr4:159027980-159027981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532956479	chr4:159028013-159028014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111216490	chr4:159028020-159028021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552928137	chr4:159028021-159028022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564840909	chr4:159028065-159028066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529412503	chr4:159028202-159028203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530561270	chr4:159028203-159028204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550383724	chr4:159028204-159028205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182637157	chr4:159028217-159028218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	20409316	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	20164919	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Autism	20841430	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:159018600-159030000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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