Variant report

Variant	esv3437386
Chromosome Location	chr6:78194283-78196031
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 176 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:176 , 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	rs16888975	chr6:78194390-78194391	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs79410101	chr6:78194393-78194394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs367718607	chr6:78194443-78194444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552729734	chr6:78194460-78194461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190899639	chr6:78194476-78194477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565104709	chr6:78194482-78194483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs10943460	chr6:78194509-78194510	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs561037946	chr6:78194515-78194516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs10664712	chr6:78194521-78194522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs181755022	chr6:78194525-78194526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs199746094	chr6:78194531-78194532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs199588919	chr6:78194532-78194533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs13213366	chr6:78194538-78194539	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs143878198	chr6:78194558-78194559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532659260	chr6:78194569-78194570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs62416459	chr6:78194573-78194574	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs200668299	chr6:78194587-78194588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186224922	chr6:78194595-78194596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12397691	chr6:78194600-78194601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559217495	chr6:78194601-78194602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375501686	chr6:78194607-78194608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189898732	chr6:78194613-78194614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs13213293	chr6:78194614-78194615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs13213598	chr6:78194627-78194628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567323124	chr6:78194630-78194631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10616763	chr6:78194641-78194642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs28394313	chr6:78194642-78194643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200713240	chr6:78194646-78194647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs28630035	chr6:78194656-78194657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556526963	chr6:78194665-78194666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200098766	chr6:78194675-78194676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141361917	chr6:78194678-78194679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs28409875	chr6:78194685-78194686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541956351	chr6:78194691-78194692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191051333	chr6:78194694-78194695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572094621	chr6:78194704-78194705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs28550486	chr6:78194707-78194708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183766338	chr6:78194714-78194715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187378585	chr6:78194720-78194721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201970537	chr6:78194728-78194729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs28607511	chr6:78194729-78194730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573017811	chr6:78194733-78194734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185090800	chr6:78194736-78194737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs367901158	chr6:78194741-78194742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558799682	chr6:78194745-78194746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187799110	chr6:78194749-78194750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529006415	chr6:78194752-78194753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192782849	chr6:78194759-78194760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184167881	chr6:78194762-78194763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189926695	chr6:78194765-78194766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Breast cancer	21990379	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:78193200-78196400	Weak transcription	HUVEC	blood vessel

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