Variant report

Variant	esv1815380
Chromosome Location	chr9:22746367-22750629
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 199 )
Associated
traits (count: 152 )

Variant overlapped rSNPs/rCNVs (count:199 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77821522	chr9:22746367-22746368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs145771451	chr9:22746373-22746374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562632325	chr9:22746392-22746393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538188600	chr9:22746401-22746402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs79304842	chr9:22746404-22746405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545170546	chr9:22746417-22746418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191633795	chr9:22746421-22746422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577158	chr9:22746438-22746439	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs140084331	chr9:22746447-22746448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542692880	chr9:22746501-22746502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184264802	chr9:22746548-22746549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs77367582	chr9:22746589-22746590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187475837	chr9:22746611-22746612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544227872	chr9:22746625-22746626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192777768	chr9:22746628-22746629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185462903	chr9:22746636-22746637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546831607	chr9:22746639-22746640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190815486	chr9:22746641-22746642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111740760	chr9:22746663-22746664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs79602144	chr9:22746698-22746699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549080850	chr9:22746699-22746700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568797967	chr9:22746729-22746730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs842845	chr9:22746734-22746735	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs367715617	chr9:22746757-22746758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs36001377	chr9:22746770-22746771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs61542557	chr9:22746771-22746772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201482312	chr9:22746772-22746773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs199626040	chr9:22746773-22746774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530825986	chr9:22746774-22746775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs202051716	chr9:22746775-22746776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200013464	chr9:22746776-22746777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201190591	chr9:22746777-22746778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201626211	chr9:22746778-22746779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375909461	chr9:22746793-22746794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200901591	chr9:22746794-22746795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200598051	chr9:22746821-22746822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569512194	chr9:22746822-22746823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577837177	chr9:22746826-22746827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551040848	chr9:22746828-22746829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571925594	chr9:22746850-22746851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534194996	chr9:22746966-22746967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs553976183	chr9:22747056-22747057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181511816	chr9:22747061-22747062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs115091125	chr9:22747083-22747084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115845430	chr9:22747097-22747098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556616508	chr9:22747151-22747152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184194802	chr9:22747194-22747195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs150333204	chr9:22747231-22747232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs842846	chr9:22747274-22747275	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs578014860	chr9:22747293-22747294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:152)

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
Glioma	20126413	CNVD
Melanoma	17363583	CNVD
Glioblastoma multiforme	19115005	CNVD
Glioblastoma multiforme	21138945	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Cancer	20581869	CNVD
Oral cancer	22144094	CNVD
Barrett''s syndrome	19417022	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
Acute myeloid leukemia	17237825	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21525872	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:22725800-22801600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr9:22738800-22778800	Weak transcription	Liver	Liver
3	chr9:22749200-22749400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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