Variant report

Variant	nsv817896
Chromosome Location	chr20:41254693-41278325
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	chr1:115296501..115298139-chr20:41277950..41280016,2	MCF-7	breast:

Extended variants
information (count: 993 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:993 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6016852	chr20:41254693-41254694	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs532507443	chr20:41254698-41254699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552705385	chr20:41254715-41254716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536074481	chr20:41254730-41254731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150572044	chr20:41254731-41254732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs535244873	chr20:41254780-41254781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184098520	chr20:41254794-41254795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187788072	chr20:41254807-41254808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537392781	chr20:41254811-41254812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576697794	chr20:41254826-41254827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557625864	chr20:41254864-41254865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs6102958	chr20:41254931-41254932	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs139565795	chr20:41254943-41254944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs73108497	chr20:41254950-41254951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552673514	chr20:41255001-41255002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs142778347	chr20:41255016-41255017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541508829	chr20:41255040-41255041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375785631	chr20:41255042-41255043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572222460	chr20:41255049-41255050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147380176	chr20:41255065-41255066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115972816	chr20:41255132-41255133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192466648	chr20:41255145-41255146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs372844990	chr20:41255149-41255150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544187809	chr20:41255179-41255180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs6030373	chr20:41255249-41255250	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs71286164	chr20:41255263-41255264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372082383	chr20:41255264-41255265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs6030375	chr20:41255266-41255267	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs559764899	chr20:41255293-41255294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528627912	chr20:41255295-41255296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548663481	chr20:41255315-41255316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs17810209	chr20:41255317-41255318	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs537614136	chr20:41255318-41255319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550995862	chr20:41255319-41255320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6030376	chr20:41255389-41255390	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs539062534	chr20:41255408-41255409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376381035	chr20:41255419-41255420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552585048	chr20:41255436-41255437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs6016853	chr20:41255484-41255485	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs535213636	chr20:41255516-41255517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555399534	chr20:41255564-41255565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575347316	chr20:41255577-41255578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144879176	chr20:41255584-41255585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs17810239	chr20:41255601-41255602	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs578022683	chr20:41255612-41255613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs6102959	chr20:41255613-41255614	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs559835482	chr20:41255620-41255621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201512469	chr20:41255643-41255644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144504368	chr20:41255646-41255647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374455025	chr20:41255647-41255648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
Autism	22495311	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	21693616	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
colon cancer	17210682	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	22028636	CNVD
Breast cancer	21264507	CNVD
Thyroid cancer	19087340	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Soft tissue tumor	16732325	CNVD
Colorectal cancer	19359472	CNVD
Gastric cancer	17167181	CNVD
Myeloproliferative neoplasm	19047681	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Oral cancer	21386901	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Ovarian cancer	19193619	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Myelodysplastic syndrome	17634407	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ductal carcinoma	22052326	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Gastric cancer	16891809	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Malignant melanoma	17260012	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Cervical cancer	21062161	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	20585902	CNVD
Ductal carcinoma	18381933	CNVD
Cancer	21129771	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	20864512	CNVD

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:41253600-41270200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr20:41257000-41258200	Enhancers	Liver	Liver
3	chr20:41263000-41263400	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr20:41263000-41264200	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr20:41270200-41270800	Enhancers	Pancreas	Pancrea
6	chr20:41270200-41271600	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr20:41271600-41300800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr20:41277000-41277400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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