Variant report

Variant	esv1831089
Chromosome Location	chr6:77436360-77452855
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 712 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:712 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534522612	chr6:77436365-77436366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552453729	chr6:77436372-77436373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs78394527	chr6:77436396-77436397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs57602829	chr6:77436421-77436422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs137987562	chr6:77436422-77436423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556732397	chr6:77436459-77436460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189907802	chr6:77436504-77436505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78182101	chr6:77436523-77436524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182126710	chr6:77436531-77436532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187147076	chr6:77436581-77436582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546083837	chr6:77436596-77436597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557665942	chr6:77436627-77436628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs111697413	chr6:77436629-77436630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs543138191	chr6:77436644-77436645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115004090	chr6:77436663-77436664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189500466	chr6:77436682-77436683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs9352377	chr6:77436710-77436711	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs549673930	chr6:77436760-77436761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143907654	chr6:77436767-77436768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs527932009	chr6:77436814-77436815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552877499	chr6:77436827-77436828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375779039	chr6:77436836-77436837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73759150	chr6:77436850-77436851	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs531964481	chr6:77436851-77436852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200840594	chr6:77436935-77436936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs35307146	chr6:77436936-77436937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs202165213	chr6:77436946-77436947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200542870	chr6:77436948-77436949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs78123922	chr6:77436949-77436950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148191460	chr6:77436969-77436970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528513396	chr6:77439211-77439212	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs112962681	chr6:77439231-77439232	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs565005045	chr6:77439264-77439265	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs4333377	chr6:77439306-77439307	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs556284811	chr6:77439327-77439328	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs2085553	chr6:77439341-77439342	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs529809408	chr6:77439377-77439378	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs548344415	chr6:77439382-77439383	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs536170067	chr6:77439393-77439394	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs566460624	chr6:77439397-77439398	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs112535369	chr6:77439404-77439405	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs535585610	chr6:77439421-77439422	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs552170113	chr6:77439427-77439428	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs571811978	chr6:77439431-77439432	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs111807323	chr6:77439475-77439476	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs544551524	chr6:77439495-77439496	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs9447754	chr6:77439497-77439498	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs575476266	chr6:77439514-77439515	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs536334218	chr6:77439518-77439519	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs2004872	chr6:77439523-77439524	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:99)

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
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	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
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	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
Ductal carcinoma	22052326	CNVD

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:77436200-77437000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr6:77439200-77441000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
3	chr6:77441000-77452800	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr6:77443200-77443600	Active TSS	Aorta	Aorta
5	chr6:77452400-77470200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:77452800-77454400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell

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