Variant report

Variant	nsv973631
Chromosome Location	chr9:44089737-44090734
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:73 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181017956	chr9:44089741-44089742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs535453612	chr9:44089767-44089768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540884088	chr9:44089769-44089770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560627501	chr9:44089791-44089792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185054335	chr9:44089799-44089800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569231167	chr9:44089801-44089802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539944221	chr9:44089812-44089813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558434324	chr9:44089820-44089821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs576979479	chr9:44089821-44089822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188692009	chr9:44089870-44089871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553303898	chr9:44089888-44089889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574828318	chr9:44089907-44089908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541829523	chr9:44089908-44089909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs140048187	chr9:44089917-44089918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs575219699	chr9:44089918-44089919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200353919	chr9:44089932-44089933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181126988	chr9:44089959-44089960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564482192	chr9:44089969-44089970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs199645079	chr9:44089980-44089981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528687331	chr9:44089997-44089998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546835604	chr9:44090010-44090011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547766983	chr9:44090011-44090012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368035191	chr9:44090012-44090013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562034821	chr9:44090013-44090014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529571423	chr9:44090045-44090046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368799274	chr9:44090047-44090048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs550534246	chr9:44090090-44090091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373510131	chr9:44090122-44090123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs377598249	chr9:44090132-44090133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569249608	chr9:44090172-44090173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370787463	chr9:44090198-44090199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551859025	chr9:44090201-44090202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375283190	chr9:44090243-44090244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370147028	chr9:44090270-44090271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs62538275	chr9:44090283-44090284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566901138	chr9:44090292-44090293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534803361	chr9:44090293-44090294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547865570	chr9:44090302-44090303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553236609	chr9:44090315-44090316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146431367	chr9:44090323-44090324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574761798	chr9:44090330-44090331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373211376	chr9:44090331-44090332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535767621	chr9:44090333-44090334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs62538276	chr9:44090347-44090348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201451470	chr9:44090355-44090356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556647109	chr9:44090370-44090371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199905169	chr9:44090389-44090390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200983954	chr9:44090392-44090393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575204073	chr9:44090402-44090403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545533044	chr9:44090424-44090425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
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
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	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
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Sezary syndrome	18413736	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	21346763	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Lung adenocarcinoma	17086460	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Lung cancer	17086460	CNVD
Rhabdomyosarcoma	16790082	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:44071000-44092000	Weak transcription	Liver	Liver

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