Variant report

Variant	esv1827034
Chromosome Location	chr16:76289715-76295598
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:59 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs386792249	chr16:76290605-76290606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs151004372	chr16:76290607-76290608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs140902300	chr16:76290623-76290624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs145934253	chr16:76290629-76290630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs193075621	chr16:76290646-76290647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556782519	chr16:76290666-76290667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563559470	chr16:76290705-76290706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369781914	chr16:76290718-76290719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs147836906	chr16:76290719-76290720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs374547491	chr16:76290727-76290728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs36012931	chr16:76290741-76290742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535975159	chr16:76290772-76290773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs376348360	chr16:76290784-76290785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs74024959	chr16:76290804-76290805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs572769964	chr16:76290836-76290837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs34202424	chr16:76290838-76290839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544694678	chr16:76290856-76290857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565532998	chr16:76290864-76290865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575852912	chr16:76290865-76290866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs373992984	chr16:76290882-76290883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs141338361	chr16:76290947-76290948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs185281459	chr16:76290950-76290951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs147052463	chr16:76290959-76290960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs369697091	chr16:76290965-76290966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs531614782	chr16:76290978-76290979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs560395338	chr16:76290995-76290996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs532494148	chr16:76291032-76291033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs190623102	chr16:76291050-76291051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs75864373	chr16:76291051-76291052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs35547349	chr16:76291083-76291084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs536988308	chr16:76291092-76291093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550343984	chr16:76291108-76291109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs567151349	chr16:76291118-76291119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs536063109	chr16:76291197-76291198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs182044730	chr16:76291320-76291321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572861959	chr16:76291342-76291343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs186456809	chr16:76291348-76291349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551360837	chr16:76291358-76291359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs4888489	chr16:76291360-76291361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs373285904	chr16:76291381-76291382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576001624	chr16:76291382-76291383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs553337488	chr16:76291394-76291395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs188095191	chr16:76291395-76291396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs561447510	chr16:76291406-76291407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs575060686	chr16:76291417-76291418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs75235573	chr16:76291420-76291421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs560584066	chr16:76291430-76291431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs180942701	chr16:76291432-76291433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573310803	chr16:76291443-76291444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs545111638	chr16:76291446-76291447	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	24585490	CNVD

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76290600-76291400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr16:76291400-76291600	Enhancers	Gastric	stomach

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