Variant report

Variant	esv1974669
Chromosome Location	chr3:76063490-76063890
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:34 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6805278	chr3:76063619-76063620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs118184740	chr3:76063620-76063621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs6793012	chr3:76063626-76063627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs6807805	chr3:76063627-76063628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs6793015	chr3:76063633-76063634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs368911974	chr3:76063640-76063641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs6805292	chr3:76063659-76063660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs6805376	chr3:76063668-76063669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs6807891	chr3:76063677-76063678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200808252	chr3:76063679-76063680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs540151454	chr3:76063682-76063683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs377489497	chr3:76063687-76063688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs376383743	chr3:76063689-76063690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189566824	chr3:76063691-76063692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs62267212	chr3:76063696-76063697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs180802049	chr3:76063699-76063700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs6767923	chr3:76063700-76063701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561982029	chr3:76063707-76063708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs572643546	chr3:76063736-76063737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs144493176	chr3:76063737-76063738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs13096614	chr3:76063738-76063739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs595047	chr3:76063754-76063755	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs6805398	chr3:76063759-76063760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533127890	chr3:76063784-76063785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs13081678	chr3:76063790-76063791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs151263094	chr3:76063792-76063793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs13077117	chr3:76063798-76063799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs551475706	chr3:76063807-76063808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs6808006	chr3:76063814-76063815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185170229	chr3:76063829-76063830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555321087	chr3:76063830-76063831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs372691715	chr3:76063853-76063854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190261894	chr3:76063855-76063856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs114810414	chr3:76063868-76063869	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	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
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Hirschsprung''s Disease	21712996	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
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Autism	22102821	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:76063600-76064200	Enhancers	Fetal Brain Male	brain

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