Variant report

Variant	nsv974457
Chromosome Location	chr14:39003070-39006649
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	chr14:38987319..38989773-chr14:39001205..39003532,2	MCF-7	breast:

Extended variants
information (count: 115 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:115 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141577106	chr14:39003109-39003110	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs541613590	chr14:39003119-39003120	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559587466	chr14:39003128-39003129	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569362582	chr14:39003134-39003135	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538299411	chr14:39003169-39003170	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558255830	chr14:39003179-39003180	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565170094	chr14:39003181-39003182	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368520882	chr14:39003194-39003195	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554149025	chr14:39003304-39003305	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574043043	chr14:39003305-39003306	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532052670	chr14:39003306-39003307	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542804931	chr14:39003337-39003338	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530251405	chr14:39003386-39003387	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562702886	chr14:39003406-39003407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576231873	chr14:39003419-39003420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544749480	chr14:39003431-39003432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs111398271	chr14:39003440-39003441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs114099098	chr14:39003476-39003477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146181859	chr14:39003514-39003515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs373548946	chr14:39003518-39003519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10530037	chr14:39003572-39003573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs72186918	chr14:39003573-39003574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374251187	chr14:39003601-39003602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200533852	chr14:39003603-39003604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201821536	chr14:39003604-39003605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs62002026	chr14:39003671-39003672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs7158163	chr14:39003672-39003673	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs530054327	chr14:39003726-39003727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530952707	chr14:39003773-39003774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140225887	chr14:39003795-39003796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569841756	chr14:39003806-39003807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570771561	chr14:39003830-39003831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187185954	chr14:39003952-39003953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7142389	chr14:39004039-39004040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571742244	chr14:39004056-39004057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147420453	chr14:39004152-39004153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534473547	chr14:39004188-39004189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533939167	chr14:39004190-39004191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530837821	chr14:39004209-39004210	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs74381288	chr14:39004218-39004219	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs201991402	chr14:39004250-39004251	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs10083444	chr14:39004284-39004285	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs17108132	chr14:39004299-39004300	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs556460623	chr14:39004318-39004319	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs77659820	chr14:39004328-39004329	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs545616223	chr14:39004395-39004396	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs117439334	chr14:39004409-39004410	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572151585	chr14:39004426-39004427	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540658761	chr14:39004460-39004461	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368338034	chr14:39004517-39004518	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:38996600-39003400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr14:39002800-39005600	Weak transcription	Fetal Brain Male	brain
3	chr14:39003000-39003400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr14:39003400-39004200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr14:39003400-39004400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr14:39004200-39004600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr14:39004400-39006000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr14:39004600-39004800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr14:39004800-39005000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr14:39005000-39006800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr14:39005000-39009000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr14:39005200-39006000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr14:39005200-39006400	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr14:39005600-39006800	Enhancers	Fetal Brain Male	brain
15	chr14:39005800-39006200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr14:39005800-39006200	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr14:39005800-39006400	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr14:39005800-39006400	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr14:39005800-39006600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr14:39006000-39006400	Enhancers	iPS-18 Cell Line	embryonic stem cell

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