Variant report

Variant	esv3342667
Chromosome Location	chr3:83025690-83026071
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:31 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552032501	chr3:83025690-83025691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs181190990	chr3:83025705-83025706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527845830	chr3:83025707-83025708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs200114942	chr3:83025710-83025711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543636222	chr3:83025717-83025718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs200178634	chr3:83025734-83025735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs9822581	chr3:83025736-83025737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201197703	chr3:83025740-83025741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs33920495	chr3:83025741-83025742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373333713	chr3:83025748-83025749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs397843386	chr3:83025749-83025750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2015857	chr3:83025750-83025751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144413752	chr3:83025758-83025759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184668269	chr3:83025761-83025762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs68087250	chr3:83025765-83025766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189990092	chr3:83025767-83025768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs35284670	chr3:83025768-83025769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs3037861	chr3:83025790-83025791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536760187	chr3:83025841-83025842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113440410	chr3:83025844-83025845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs570011140	chr3:83025872-83025873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs1986098	chr3:83025873-83025874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558855340	chr3:83025880-83025881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572391352	chr3:83025897-83025898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181688351	chr3:83025909-83025910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538492256	chr3:83025922-83025923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373270968	chr3:83025934-83025935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs386662975	chr3:83025993-83025994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs62259959	chr3:83025994-83025995	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs567646465	chr3:83025998-83025999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532120187	chr3:83026012-83026013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
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
Acute myeloid leukemia	20729466	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
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
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	17124404	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Autism	20808228	CNVD
Urothelial carcinoma	21177765	CNVD
Neurodevelopmental disorder	22521361	CNVD
Medulloblastoma	16783165	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:83023400-83027000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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