Variant report

Variant	nsv969784
Chromosome Location	chr9:24096444-24109521
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 141 )

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141378670	chr9:24096452-24096453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs193267992	chr9:24096459-24096460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs10966206	chr9:24096480-24096481	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs530635974	chr9:24096499-24096500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs111756727	chr9:24096577-24096578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550421517	chr9:24096610-24096611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs76402625	chr9:24096616-24096617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs570658460	chr9:24096617-24096618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs377175210	chr9:24096618-24096619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs112544325	chr9:24096628-24096629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs531089514	chr9:24096651-24096652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs138338811	chr9:24096689-24096690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs376682301	chr9:24096699-24096700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566494877	chr9:24096759-24096760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs78695124	chr9:24096811-24096812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555520573	chr9:24096817-24096818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568633930	chr9:24096819-24096820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs143825037	chr9:24096839-24096840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs557580756	chr9:24096842-24096843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs147234431	chr9:24096899-24096900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs139778466	chr9:24096930-24096931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs185438209	chr9:24096937-24096938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188972071	chr9:24096982-24096983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs74987552	chr9:24096989-24096990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149369321	chr9:24096990-24096991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192296830	chr9:24097003-24097004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs544071567	chr9:24097017-24097018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs184499383	chr9:24097032-24097033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs144805546	chr9:24097033-24097034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372626651	chr9:24097038-24097039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs74386442	chr9:24097039-24097040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560160575	chr9:24097050-24097051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs13300305	chr9:24097087-24097088	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs74951563	chr9:24097095-24097096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs568973232	chr9:24097105-24097106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs188860747	chr9:24097118-24097119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs550881653	chr9:24097130-24097131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571054933	chr9:24097190-24097191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs539717260	chr9:24097196-24097197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs148554570	chr9:24097201-24097202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs10966207	chr9:24097219-24097220	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs117367576	chr9:24097226-24097227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs181105949	chr9:24097268-24097269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs575324628	chr9:24097284-24097285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs116443691	chr9:24097324-24097325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs564102072	chr9:24097328-24097329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs144557665	chr9:24097337-24097338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs184522280	chr9:24097359-24097360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs189044367	chr9:24097367-24097368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs529253762	chr9:24097382-24097383	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:141)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Glioblastoma multiforme	21569311	CNVD
Myelofibrosis	22110671	CNVD
Ewing''s sarcoma	22429812	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	19435819	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Lung cancer	21911935	CNVD
Primary central nervous system lymphoma	21088137	CNVD
head and neck squamous cell carcinoma	21798897	CNVD
Cancer	21253487	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Urothelial cell carcinoma	18451213	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Leukemia	19602459	CNVD
Acute monocytic leukemia	16498392	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Leukemia	18688285	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Acute myeloid leukemia	19651601	CNVD
Coronary Disease	20032323	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21732550	CNVD
Gastric cancer	22539939	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Metastatic melanoma	18483359	CNVD
Non-small cell lung cancer	20864512	CNVD
Cervical cancer	21062161	CNVD
Acute myeloid leukemia	16864856	CNVD
Glioblastoma	17090523	CNVD
Lung cancer	16773561	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16774939	CNVD
Bladder cancer	19088036	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	16977458	CNVD
Glioblastoma multiforme	17369134	CNVD
Chagasic megaesophagus	20163722	CNVD
Melanoma	19566914	CNVD
Squamous cell cancer	19047905	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Melanoma	17363583	CNVD
Glioblastoma multiforme	19115005	CNVD
Adenoid cystic carcinoma	18332873	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:24095600-24096600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr9:24096600-24097400	Enhancers	Primary hematopoietic stem cells short term culture	blood

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