Variant report

Variant	nsv1021934
Chromosome Location	chr6:66393348-66403840
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	chr3:189034137..189034728-chr6:66401890..66402666,2	MCF-7	breast:
2	chr6:66389053..66391661-chr6:66392622..66394298,2	MCF-7	breast:

Extended variants
information (count: 223 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:223 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4710534	chr6:66393348-66393349	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572654589	chr6:66393350-66393351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs190080565	chr6:66393491-66393492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562032557	chr6:66393505-66393506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs531068632	chr6:66393534-66393535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs550679543	chr6:66393635-66393636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564447074	chr6:66393639-66393640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs111741416	chr6:66393668-66393669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs547277240	chr6:66393708-66393709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181631168	chr6:66393738-66393739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184649161	chr6:66393756-66393757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536074659	chr6:66393760-66393761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189481919	chr6:66393950-66393951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs146058775	chr6:66393974-66393975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568038427	chr6:66394057-66394058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs9294645	chr6:66394090-66394091	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs79527468	chr6:66394110-66394111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143465982	chr6:66394127-66394128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534096371	chr6:66394135-66394136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539048438	chr6:66394150-66394151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10944833	chr6:66394158-66394159	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs572842603	chr6:66394173-66394174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541644910	chr6:66394176-66394177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs16897048	chr6:66394196-66394197	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs114902360	chr6:66394209-66394210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs180826594	chr6:66394212-66394213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564582591	chr6:66394215-66394216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185962409	chr6:66394244-66394245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs61422784	chr6:66394252-66394253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560749662	chr6:66394256-66394257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs75287117	chr6:66394259-66394260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549431333	chr6:66394273-66394274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191259367	chr6:66394280-66394281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146734395	chr6:66394281-66394282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550213210	chr6:66394302-66394303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs139132330	chr6:66394312-66394313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539037873	chr6:66394330-66394331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552584960	chr6:66394339-66394340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149908773	chr6:66394361-66394362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535713592	chr6:66394366-66394367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555392357	chr6:66394386-66394387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs116306439	chr6:66394392-66394393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533610936	chr6:66394393-66394394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558282833	chr6:66394440-66394441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144923381	chr6:66394464-66394465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200427782	chr6:66394490-66394491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540606965	chr6:66394535-66394536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560482841	chr6:66394544-66394545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529284591	chr6:66394551-66394552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543264301	chr6:66394583-66394584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Ovarian cancer	19835627	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	20164919	CNVD
Retinitis pigmentosa	21519034	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:66392800-66393800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr6:66393800-66396000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr6:66396000-66396200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:66396200-66396600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr6:66399600-66400400	Enhancers	Placenta	Placenta
6	chr6:66401800-66402200	Enhancers	Rectal Mucosa Donor 29	rectum
7	chr6:66402200-66403400	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr6:66403600-66403800	Enhancers	Rectal Mucosa Donor 29	rectum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links