Variant report

Variant	esv2236053
Chromosome Location	chr8:52367315-52367896
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 86 )

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	rs73581425	chr8:52367444-52367445	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567601458	chr8:52367451-52367452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs16916332	chr8:52367473-52367474	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs74850039	chr8:52367482-52367483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370863538	chr8:52367517-52367518	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs369154988	chr8:52367518-52367519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs117620782	chr8:52367529-52367530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs578130706	chr8:52367532-52367533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563999483	chr8:52367586-52367587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557110879	chr8:52367598-52367599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575358353	chr8:52367654-52367655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533064155	chr8:52367670-52367671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543405827	chr8:52367671-52367672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536468204	chr8:52367675-52367676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs71237210	chr8:52367693-52367694	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs78003211	chr8:52367746-52367747	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563278356	chr8:52367792-52367793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528941078	chr8:52367832-52367833	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188745117	chr8:52367894-52367895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:52355400-52374000	Weak transcription	Right Ventricle	heart
2	chr8:52356800-52396200	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr8:52365800-52369200	Enhancers	Primary B cells from peripheral blood	blood
4	chr8:52366200-52374000	Weak transcription	Right Atrium	heart
5	chr8:52366400-52374000	Weak transcription	Left Ventricle	heart
6	chr8:52367000-52367800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr8:52367800-52368400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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