Variant report

Variant	esv3383374
Chromosome Location	chr3:55810707-55811121
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143549010	chr3:55810719-55810720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs555485451	chr3:55810720-55810721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148044529	chr3:55810748-55810749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs9866297	chr3:55810766-55810767	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs112225406	chr3:55810811-55810812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs141674196	chr3:55810819-55810820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187858210	chr3:55810868-55810869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115212332	chr3:55810877-55810878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs145977645	chr3:55810917-55810918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs12631767	chr3:55810929-55810930	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs79389315	chr3:55810930-55810931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531447382	chr3:55810943-55810944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551555207	chr3:55810961-55810962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565112432	chr3:55810972-55810973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138510920	chr3:55810998-55810999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566976194	chr3:55811058-55811059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs547696427	chr3:55811060-55811061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs113261536	chr3:55811104-55811105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550735913	chr3:55811105-55811106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566746887	chr3:55811106-55811107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs202213543	chr3:55811112-55811113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368344902	chr3:55811114-55811115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184507811	chr3:55811118-55811119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs189645256	chr3:55811121-55811122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Renal cell carcinoma	18765545	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:55810600-55816200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:55811000-55811400	Enhancers	Fetal Stomach	stomach

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