Variant report

Variant	esv3367493
Chromosome Location	chr6:101754831-101758929
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546878177	chr6:101754831-101754832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs553709700	chr6:101754847-101754848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184650340	chr6:101754866-101754867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572159824	chr6:101754884-101754885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs283229	chr6:101754901-101754902	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs558125467	chr6:101754910-101754911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576403199	chr6:101754920-101754921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544644618	chr6:101754929-101754930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs539174170	chr6:101754934-101754935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189971385	chr6:101754935-101754936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs60911697	chr6:101754942-101754943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs202226131	chr6:101754948-101754949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs283228	chr6:101754993-101754994	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs542281636	chr6:101755064-101755065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs535556339	chr6:101755117-101755118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs560520915	chr6:101755166-101755167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527843882	chr6:101755168-101755169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552484425	chr6:101755176-101755177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs283227	chr6:101755248-101755249	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs531870626	chr6:101755259-101755260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs375403186	chr6:101755276-101755277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567692896	chr6:101755323-101755324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs71566369	chr6:101755324-101755325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535204860	chr6:101755365-101755366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs117752780	chr6:101755396-101755397	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17170743	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21785460	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Obesity	21045960	CNVD
Liver carcinoma	19366792	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Urothelial carcinoma	21177765	CNVD
Autism	22543975	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:101754800-101755000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:101755000-101755400	Enhancers	Muscle Satellite Cultured Cells	--

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