Variant report

Variant	nsv982107
Chromosome Location	chr8:89514721-89530521
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:89513243..89515603-chr8:89516422..89518652,2	MCF-7	breast:
2	chr8:89513243..89515603-chr8:89516422..89518652,2	MCF-7	breast:

Extended variants
information (count: 41 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:41 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548601068	chr8:89521614-89521615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs569957434	chr8:89521650-89521651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530985663	chr8:89521654-89521655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs367837399	chr8:89521666-89521667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552723780	chr8:89521668-89521669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs1906448	chr8:89521729-89521730	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs538869728	chr8:89521753-89521754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs11986130	chr8:89521773-89521774	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs566025810	chr8:89521832-89521833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189126856	chr8:89521889-89521890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141338605	chr8:89521920-89521921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs527995661	chr8:89521929-89521930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs373673676	chr8:89521938-89521939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs59759655	chr8:89521982-89521983	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs145094698	chr8:89522002-89522003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558248444	chr8:89522054-89522055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs117803838	chr8:89522089-89522090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs541257493	chr8:89522100-89522101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181068943	chr8:89522115-89522116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs57195479	chr8:89522150-89522151	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs185507825	chr8:89522192-89522193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs182102030	chr8:89527802-89527803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542877084	chr8:89527901-89527902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs185172770	chr8:89527905-89527906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551163060	chr8:89527930-89527931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs543693178	chr8:89527998-89527999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs565266135	chr8:89528068-89528069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189830254	chr8:89528088-89528089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs111801905	chr8:89528109-89528110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs547813180	chr8:89528125-89528126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs565952186	chr8:89528126-89528127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs569318258	chr8:89528136-89528137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs182483366	chr8:89528137-89528138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs548418749	chr8:89528144-89528145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs16883962	chr8:89528148-89528149	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs538063606	chr8:89528159-89528160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs570699315	chr8:89528169-89528170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs10504863	chr8:89528229-89528230	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs146832956	chr8:89528267-89528268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs571108036	chr8:89528299-89528300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538943235	chr8:89528315-89528316	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:89521600-89522200	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr8:89527800-89528400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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