Variant report

Variant	esv3423015
Chromosome Location	chr2:231426560-231426972
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35637946	chr2:231426564-231426565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs77635808	chr2:231426575-231426576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs62195486	chr2:231426580-231426581	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs571112171	chr2:231426590-231426591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs181866142	chr2:231426611-231426612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530272512	chr2:231426634-231426635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186937186	chr2:231426683-231426684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs566538638	chr2:231426729-231426730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190425648	chr2:231426736-231426737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539704746	chr2:231426810-231426811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs145961316	chr2:231426878-231426879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182496580	chr2:231426899-231426900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113445425	chr2:231426900-231426901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570121243	chr2:231426909-231426910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs139921823	chr2:231426937-231426938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs202170739	chr2:231426949-231426950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs67439016	chr2:231426956-231426957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1616037	chr2:231426958-231426959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554674692	chr2:231426960-231426961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs572977643	chr2:231426962-231426963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540313078	chr2:231426964-231426965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs76157442	chr2:231426966-231426967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	22429812	CNVD
Bladder cancer	21909424	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
prenatal diagnosis	22389664	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mental retardation	20152051	CNVD
Cancer	21183584	CNVD
Albright''s disease	22277900	CNVD
Brachydactyly-Mental Retardation Syndrome	22470819	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Colorectal cancer	19359472	CNVD
Autism	18414403	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:231401000-231430200	Weak transcription	Pancreas	Pancrea
2	chr2:231410200-231428800	Weak transcription	Primary B cells from cord blood	blood
3	chr2:231426600-231427200	Enhancers	Primary B cells from peripheral blood	blood

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