Variant report

Variant	nsv887621
Chromosome Location	chr7:11916354-11950061
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 589 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375966146	chr7:11926008-11926009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs551492914	chr7:11926051-11926052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571249281	chr7:11926077-11926078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs537102729	chr7:11926089-11926090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557282011	chr7:11926094-11926095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192648489	chr7:11926108-11926109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs34470996	chr7:11926203-11926204	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs55871489	chr7:11926209-11926210	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs377140409	chr7:11926214-11926215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553682545	chr7:11926240-11926241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs9655089	chr7:11926256-11926257	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs9655090	chr7:11926263-11926264	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs10269434	chr7:11926305-11926306	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs575655801	chr7:11926329-11926330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs9655091	chr7:11926347-11926348	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs184087380	chr7:11926356-11926357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142540831	chr7:11926357-11926358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs10242909	chr7:11926366-11926367	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs368459253	chr7:11926378-11926379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs2355135	chr7:11926424-11926425	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs528120323	chr7:11926458-11926459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561098074	chr7:11926488-11926489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs2355136	chr7:11926503-11926504	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs10229285	chr7:11926516-11926517	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs550621419	chr7:11926544-11926545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567888057	chr7:11926549-11926550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs117288293	chr7:11926564-11926565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553743935	chr7:11926570-11926571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs10272955	chr7:11926573-11926574	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs372113898	chr7:11926581-11926582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs10243182	chr7:11926585-11926586	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs11771848	chr7:11927254-11927255	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs538227125	chr7:11927273-11927274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs554687040	chr7:11927274-11927275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs531735111	chr7:11927300-11927301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs183638550	chr7:11927315-11927316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs533987889	chr7:11927361-11927362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs552764901	chr7:11927374-11927375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs139183740	chr7:11927393-11927394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546993037	chr7:11927642-11927643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs10277256	chr7:11927672-11927673	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs141823344	chr7:11927710-11927711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539021009	chr7:11927711-11927712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs11772691	chr7:11927729-11927730	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs139948272	chr7:11927756-11927757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143429252	chr7:11927758-11927759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569371021	chr7:11927759-11927760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146241212	chr7:11927780-11927781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10277171	chr7:11927782-11927783	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs117365002	chr7:11927820-11927821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	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
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Autism	22495309	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:11926000-11926600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:11927200-11927400	Enhancers	H1 Cell Line	embryonic stem cell
3	chr7:11927600-11930800	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr7:11927600-11931800	Weak transcription	Pancreas	Pancrea
5	chr7:11930800-11931600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
6	chr7:11931600-11932600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr7:11931800-11932000	ZNF genes & repeats	Pancreas	Pancrea
8	chr7:11932600-11933000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr7:11934600-11935200	Enhancers	Fetal Brain Female	brain
10	chr7:11935400-11936200	Enhancers	Fetal Brain Male	brain
11	chr7:11935800-11936800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr7:11936200-11936800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr7:11936800-11937200	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr7:11937200-11937400	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr7:11937400-11940200	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr7:11940000-11941000	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr7:11940200-11941200	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr7:11940600-11941000	Enhancers	H1 Cell Line	embryonic stem cell
19	chr7:11940600-11941200	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr7:11940800-11941200	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr7:11950000-11950800	Enhancers	Hela-S3	cervix

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