Variant report

Variant	esv3476004
Chromosome Location	chr7:39869962-39870428
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73132704	chr7:39870019-39870020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs60023431	chr7:39870049-39870050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs79581606	chr7:39870050-39870051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565576929	chr7:39870052-39870053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs397947835	chr7:39870063-39870064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs75276110	chr7:39870064-39870065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs372050278	chr7:39870068-39870069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs373338380	chr7:39870085-39870086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs12667771	chr7:39870095-39870096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556397560	chr7:39870175-39870176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs188067645	chr7:39870249-39870250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370343177	chr7:39870255-39870256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181034169	chr7:39870272-39870273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs545339595	chr7:39870296-39870297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549762608	chr7:39870332-39870333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs60588694	chr7:39870339-39870340	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs546779888	chr7:39870363-39870364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs7776988	chr7:39870382-39870383	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs538637872	chr7:39870389-39870390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
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
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	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
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Gastric cancer	24379144	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Bladder cancer	21909424	CNVD

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39866600-39872400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr7:39866800-39872400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links