Variant report

Variant	nsv1033852
Chromosome Location	chr7:19506544-19517086
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	chr7:19502491..19504536-chr7:19508124..19510768,2	K562	blood:

Extended variants
information (count: 88 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:88 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17141358	chr7:19506544-19506545	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs548654354	chr7:19506552-19506553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs138507690	chr7:19506595-19506596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577350805	chr7:19506600-19506601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs116832338	chr7:19506616-19506617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs537431656	chr7:19506657-19506658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs559339021	chr7:19506703-19506704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs117470155	chr7:19506708-19506709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs139216498	chr7:19506744-19506745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553553976	chr7:19506750-19506751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574890230	chr7:19506782-19506783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571780401	chr7:19506796-19506797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541919206	chr7:19506808-19506809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556631097	chr7:19506854-19506855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs200122509	chr7:19506874-19506875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs182183184	chr7:19506908-19506909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs566481146	chr7:19506935-19506936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs17141363	chr7:19506961-19506962	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs528400328	chr7:19506997-19506998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76746515	chr7:19507044-19507045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs111357127	chr7:19507051-19507052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs111392316	chr7:19507052-19507053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs543810285	chr7:19507074-19507075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs368503616	chr7:19507086-19507087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs144090763	chr7:19507110-19507111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs548739461	chr7:19507121-19507122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs193209015	chr7:19507135-19507136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs114630879	chr7:19509831-19509832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549814733	chr7:19509849-19509850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs571231585	chr7:19509860-19509861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs2110470	chr7:19509870-19509871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553996414	chr7:19509887-19509888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565779576	chr7:19509920-19509921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs184519203	chr7:19509939-19509940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs368953044	chr7:19509966-19509967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs533832227	chr7:19510025-19510026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs536445258	chr7:19510032-19510033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555471144	chr7:19510047-19510048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs148479784	chr7:19510049-19510050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs544266318	chr7:19510072-19510073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs555273818	chr7:19510073-19510074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs144175547	chr7:19510117-19510118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs189080091	chr7:19510135-19510136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs77125108	chr7:19510169-19510170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs78970236	chr7:19511472-19511473	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs75863573	chr7:19511479-19511480	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs148216787	chr7:19511498-19511499	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs2024350	chr7:19511572-19511573	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs199938656	chr7:19511577-19511578	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs116374105	chr7:19511583-19511584	Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:19504400-19507200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr7:19506000-19506800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr7:19509800-19510200	Enhancers	Muscle Satellite Cultured Cells	--
4	chr7:19511400-19511800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
5	chr7:19513000-19513400	Enhancers	Pancreatic Islets	Pancreatic Islet

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