Variant report

Variant	esv11031
Chromosome Location	chr1:191726014-191727002
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:191720033..191721818-chr1:191724258..191727232,2	K562	blood:
2	chr1:191722550..191725173-chr1:191726760..191728509,2	K562	blood:
3	chr1:191716548..191718884-chr1:191723444..191727562,3	K562	blood:

Extended variants
information (count: 46 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:46 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545843598	chr1:191726037-191726038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557608658	chr1:191726140-191726141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs833968	chr1:191726158-191726159	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs147789651	chr1:191726200-191726201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs186058080	chr1:191726315-191726316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557275543	chr1:191726319-191726320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs191105423	chr1:191726340-191726341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs367951593	chr1:191726380-191726381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs542962086	chr1:191726413-191726414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559539955	chr1:191726473-191726474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545003569	chr1:191726533-191726534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577277163	chr1:191726550-191726551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs544714929	chr1:191726570-191726571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs572964876	chr1:191726583-191726584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs372078076	chr1:191726627-191726628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs200781278	chr1:191726662-191726663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs372673368	chr1:191726672-191726673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs12760758	chr1:191726673-191726674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs12742124	chr1:191726675-191726676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369039681	chr1:191726677-191726678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs373399147	chr1:191726679-191726680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376842689	chr1:191726681-191726682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs142894113	chr1:191726683-191726684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs71522445	chr1:191726684-191726685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs111551546	chr1:191726685-191726686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs369907933	chr1:191726687-191726688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373506187	chr1:191726689-191726690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376769178	chr1:191726691-191726692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs369093389	chr1:191726693-191726694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs373889141	chr1:191726695-191726696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs71107467	chr1:191726703-191726704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182087695	chr1:191726716-191726717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs116086162	chr1:191726718-191726719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs114844776	chr1:191726720-191726721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs185498816	chr1:191726748-191726749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs543446626	chr1:191726765-191726766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs563358377	chr1:191726834-191726835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs529517455	chr1:191726838-191726839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs549275214	chr1:191726895-191726896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs566253437	chr1:191726917-191726918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs373613109	chr1:191726938-191726939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs369080493	chr1:191726942-191726943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs189919923	chr1:191726953-191726954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373651321	chr1:191726979-191726980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs369600898	chr1:191726980-191726981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs551433848	chr1:191726988-191726989	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	17086460	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	17086460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:191725600-191726600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr1:191725600-191727000	Enhancers	Dnd41	blood
3	chr1:191725800-191726600	Enhancers	K562	blood

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