Variant report

Variant	esv2587357
Chromosome Location	chr12:58509475-58514805
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 92 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:92 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562793549	chr12:58510823-58510824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs533108783	chr12:58510824-58510825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551333564	chr12:58510832-58510833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566314538	chr12:58510833-58510834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139759847	chr12:58510837-58510838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571220196	chr12:58510965-58510966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549058367	chr12:58511013-58511014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150073936	chr12:58511037-58511038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs536051772	chr12:58511046-58511047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs557311386	chr12:58511060-58511061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs11334700	chr12:58511079-58511080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs397805445	chr12:58511094-58511095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs376505050	chr12:58511095-58511096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs144385563	chr12:58511125-58511126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539717339	chr12:58511130-58511131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558443119	chr12:58511152-58511153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs73095874	chr12:58511156-58511157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148780015	chr12:58511195-58511196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs187555068	chr12:58511250-58511251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573838753	chr12:58511274-58511275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs373758059	chr12:58511306-58511307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543989118	chr12:58511324-58511325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs562567637	chr12:58511380-58511381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs193110279	chr12:58511408-58511409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs142388201	chr12:58511484-58511485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs560402077	chr12:58511512-58511513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs527238496	chr12:58511538-58511539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111242717	chr12:58511543-58511544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549045881	chr12:58511544-58511545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs11172466	chr12:58511607-58511608	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs200830034	chr12:58511654-58511655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs11612088	chr12:58511670-58511671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs533908360	chr12:58511683-58511684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs141606757	chr12:58511691-58511692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540034030	chr12:58511733-58511734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs551740606	chr12:58511735-58511736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs566871863	chr12:58511737-58511738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533925843	chr12:58511792-58511793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs539968488	chr12:58513049-58513050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs145344328	chr12:58513076-58513077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs527892778	chr12:58513112-58513113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs549222280	chr12:58513127-58513128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs567619346	chr12:58513163-58513164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs562604600	chr12:58513204-58513205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531604652	chr12:58513212-58513213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs11613082	chr12:58513237-58513238	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs571633680	chr12:58513291-58513292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs111256825	chr12:58513307-58513308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs539149546	chr12:58513326-58513327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs533151928	chr12:58513343-58513344	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Bladder cancer	21909424	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Autism	20531469	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21138945	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21364760	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:58510800-58511400	Enhancers	Dnd41	blood
2	chr12:58511400-58511800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr12:58513000-58514000	Enhancers	Ovary	ovary
4	chr12:58514000-58514200	Enhancers	Psoas Muscle	Psoas
5	chr12:58514000-58517000	Weak transcription	Ovary	ovary
6	chr12:58514200-58517000	Weak transcription	Psoas Muscle	Psoas
7	chr12:58514400-58514800	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr12:58514400-58515000	Enhancers	iPS-15b Cell Line	embryonic stem cell

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