Variant report

Variant	esv1963446
Chromosome Location	chr7:38580697-38581133
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191134169	chr7:38580697-38580698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs12155369	chr7:38580704-38580705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569193881	chr7:38580726-38580727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs368765374	chr7:38580769-38580770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113519991	chr7:38580796-38580797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs144543093	chr7:38580824-38580825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs55660201	chr7:38580832-38580833	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs527575056	chr7:38580860-38580861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553733190	chr7:38580862-38580863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183357861	chr7:38580863-38580864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs188050805	chr7:38580885-38580886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs374726557	chr7:38580888-38580889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs372772703	chr7:38580889-38580890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs3839745	chr7:38580890-38580891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs78443763	chr7:38580928-38580929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs536060013	chr7:38580980-38580981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191983942	chr7:38580984-38580985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146603987	chr7:38581044-38581045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76309521	chr7:38581048-38581049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546728419	chr7:38581056-38581057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs549344159	chr7:38581105-38581106	Weak transcription Enhancers	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
Gastrointestinal stromal cancer	20818650	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
Sezary syndrome	18413736	CNVD
Gastric cancer	24379144	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38564200-38580800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr7:38579400-38586800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr7:38580200-38581200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr7:38580600-38581800	Enhancers	Fetal Heart	heart
5	chr7:38580600-38583800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr7:38580600-38583800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr7:38580800-38581400	Enhancers	Sigmoid Colon	Sigmoid Colon
8	chr7:38580800-38581800	Enhancers	Left Ventricle	heart
9	chr7:38580800-38582200	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr7:38581000-38581600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr7:38581000-38581800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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