Variant report

Variant	nsv1030846
Chromosome Location	chr7:16015341-16028125
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 500 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:500 , 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	rs10486788	chr7:16015341-16015342	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs79585639	chr7:16015376-16015377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs529178213	chr7:16015390-16015391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs555696929	chr7:16015464-16015465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs116184972	chr7:16015481-16015482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538298610	chr7:16015570-16015571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs554033345	chr7:16015605-16015606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572279297	chr7:16015609-16015610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183639612	chr7:16015656-16015657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188446345	chr7:16015661-16015662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576578107	chr7:16015702-16015703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543936657	chr7:16015711-16015712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148728350	chr7:16015723-16015724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565091981	chr7:16015783-16015784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532527829	chr7:16015789-16015790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541111773	chr7:16015848-16015849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2052028	chr7:16015863-16015864	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs118118289	chr7:16015867-16015868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548337852	chr7:16015896-16015897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs117924007	chr7:16015970-16015971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181255984	chr7:16015988-16015989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549458816	chr7:16016008-16016009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs571304036	chr7:16016009-16016010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552348608	chr7:16016033-16016034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553522970	chr7:16016058-16016059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565932069	chr7:16016062-16016063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551368431	chr7:16016123-16016124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185114085	chr7:16016145-16016146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs144238948	chr7:16016159-16016160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576313406	chr7:16016180-16016181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543682387	chr7:16016182-16016183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190356358	chr7:16016256-16016257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148707401	chr7:16016260-16016261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs377667205	chr7:16016306-16016307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10268779	chr7:16016336-16016337	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs528572234	chr7:16016348-16016349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375198181	chr7:16016367-16016368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs142360874	chr7:16016397-16016398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530298081	chr7:16016411-16016412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542129212	chr7:16016426-16016427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563681196	chr7:16016428-16016429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531008561	chr7:16016433-16016434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552527142	chr7:16016436-16016437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571305352	chr7:16016438-16016439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146340502	chr7:16016467-16016468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs34706043	chr7:16016479-16016480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547341476	chr7:16016482-16016483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs1918857	chr7:16016504-16016505	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs536773558	chr7:16016515-16016516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139603289	chr7:16016552-16016553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	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
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
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16013200-16017000	Weak transcription	Osteobl	bone
2	chr7:16013200-16017400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr7:16013200-16017400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr7:16013200-16017400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr7:16013200-16017400	Weak transcription	NHDF-Ad	bronchial
6	chr7:16013400-16016800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr7:16013400-16017200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr7:16013800-16017000	Weak transcription	HUVEC	blood vessel
9	chr7:16014400-16015600	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr7:16015400-16015600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr7:16016800-16018000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr7:16017000-16017800	Enhancers	Osteobl	bone
13	chr7:16017000-16018200	Enhancers	HUVEC	blood vessel
14	chr7:16017200-16017800	Enhancers	Muscle Satellite Cultured Cells	--
15	chr7:16017200-16018000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr7:16017400-16017800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr7:16017400-16017800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr7:16017400-16017800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr7:16017400-16017800	Enhancers	NHDF-Ad	bronchial
20	chr7:16020200-16024200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr7:16020400-16023800	Weak transcription	Left Ventricle	heart
22	chr7:16024200-16024400	Enhancers	Left Ventricle	heart
23	chr7:16024200-16024800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr7:16024400-16026600	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr7:16024400-16027000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr7:16024600-16025800	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr7:16024600-16026000	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr7:16024600-16027000	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr7:16024800-16025600	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr7:16024800-16027000	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr7:16024800-16027200	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr7:16025400-16025600	Enhancers	NHDF-Ad	bronchial
33	chr7:16025600-16026000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr7:16025600-16026000	Enhancers	Fetal Brain Male	brain
35	chr7:16025600-16026000	Flanking Active TSS	NHDF-Ad	bronchial
36	chr7:16026000-16026200	Enhancers	NHDF-Ad	bronchial
37	chr7:16026200-16026400	Flanking Active TSS	NHDF-Ad	bronchial
38	chr7:16027000-16027400	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr7:16027400-16027800	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr7:16027400-16029200	Enhancers	Breast Myoepithelial Primary Cells	Breast

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