Variant report

Variant	esv3433864
Chromosome Location	chr9:17587031-17587748
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:34 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576944123	chr9:17587033-17587034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs554167961	chr9:17587043-17587044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116082042	chr9:17587045-17587046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs73418627	chr9:17587059-17587060	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs541191124	chr9:17587105-17587106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554788033	chr9:17587131-17587132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576182573	chr9:17587132-17587133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149614977	chr9:17587160-17587161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565227869	chr9:17587166-17587167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577163359	chr9:17587178-17587179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530283354	chr9:17587228-17587229	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs7867956	chr9:17587254-17587255	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs559333228	chr9:17587327-17587328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs148753445	chr9:17587339-17587340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181195583	chr9:17587342-17587343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563384669	chr9:17587356-17587357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185063423	chr9:17587383-17587384	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs58929042	chr9:17587419-17587420	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs189944698	chr9:17587423-17587424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74953463	chr9:17587438-17587439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs76731282	chr9:17587499-17587500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs78506578	chr9:17587500-17587501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549590143	chr9:17587515-17587516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114369064	chr9:17587527-17587528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs75636432	chr9:17587564-17587565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs79096476	chr9:17587612-17587613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs147450715	chr9:17587620-17587621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554603086	chr9:17587641-17587642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200877610	chr9:17587650-17587651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs139891055	chr9:17587657-17587658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376973061	chr9:17587676-17587677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs6475153	chr9:17587687-17587688	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs6475154	chr9:17587703-17587704	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs142167999	chr9:17587737-17587738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
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
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
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	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
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	21364760	CNVD
Cancer	22183965	CNVD
Lung adenocarcinoma	21935476	CNVD
Thoracic aortic aneurysm	21698135	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17580800-17589600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr9:17581400-17590000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr9:17585800-17589600	Weak transcription	Fetal Brain Female	brain
4	chr9:17587200-17587400	Enhancers	H1 Cell Line	embryonic stem cell

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