Variant report

Variant	nsv1002414
Chromosome Location	chr3:89394580-89408423
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	chr3:89374528..89377645-chr3:89392593..89395332,3	MCF-7	breast:

Extended variants
information (count: 451 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:451 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577045229	chr3:89394581-89394582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs537477444	chr3:89394584-89394585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141639852	chr3:89394647-89394648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186447062	chr3:89394648-89394649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541956516	chr3:89394665-89394666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191275702	chr3:89394666-89394667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560255903	chr3:89394682-89394683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573500960	chr3:89394706-89394707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540800700	chr3:89394745-89394746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528144226	chr3:89394756-89394757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369063829	chr3:89394757-89394758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs9823081	chr3:89394769-89394770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs9843016	chr3:89394770-89394771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565477221	chr3:89394779-89394780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs375284403	chr3:89394840-89394841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs111477928	chr3:89394845-89394846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550742575	chr3:89394846-89394847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs61263861	chr3:89394856-89394857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566171244	chr3:89394872-89394873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529995618	chr3:89394873-89394874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548289302	chr3:89394878-89394879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566597774	chr3:89394900-89394901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9843305	chr3:89394917-89394918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs9823398	chr3:89394918-89394919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533765313	chr3:89395012-89395013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370630907	chr3:89395034-89395035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570694966	chr3:89395035-89395036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538146761	chr3:89395063-89395064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556143771	chr3:89395087-89395088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574501575	chr3:89395089-89395090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374749854	chr3:89395090-89395091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546725996	chr3:89395120-89395121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs367794144	chr3:89395170-89395171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201194430	chr3:89395202-89395203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112386624	chr3:89395214-89395215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111238708	chr3:89395217-89395218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs370101785	chr3:89395264-89395265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62275012	chr3:89395403-89395404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373637553	chr3:89395425-89395426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs368709150	chr3:89395486-89395487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372626406	chr3:89395633-89395634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535413694	chr3:89395768-89395769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553938519	chr3:89395797-89395798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572157478	chr3:89395809-89395810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375571904	chr3:89396000-89396001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs202124829	chr3:89396007-89396008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545787085	chr3:89396692-89396693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540514576	chr3:89396754-89396755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565474236	chr3:89397051-89397052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577317046	chr3:89397069-89397070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Soft tissue tumor	16732325	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
craniofacial dysmorphism	21918468	CNVD
Cancer	20164920	CNVD
Non-small cell lung cancer	21829676	CNVD
Lung cancer	19547694	CNVD
Cancer	20164919	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:89392600-89417400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr3:89394400-89394600	Enhancers	Fetal Brain Female	brain
3	chr3:89400200-89401000	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr3:89400200-89401000	Active TSS	iPS-15b Cell Line	embryonic stem cell
5	chr3:89400600-89401000	Active TSS	HUES6 Cell Line	embryonic stem cell
6	chr3:89401000-89401200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr3:89401000-89401200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr3:89402200-89403200	Enhancers	Hela-S3	cervix
9	chr3:89404400-89417600	Weak transcription	Brain Germinal Matrix	brain
10	chr3:89407400-89407600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr3:89407800-89409000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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