Variant report

Variant	nsv573027
Chromosome Location	chr16:76443174-76451242
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 83 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:83 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1506833	chr16:76443174-76443175	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs115792628	chr16:76443185-76443186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566904427	chr16:76443208-76443209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs34516314	chr16:76443238-76443239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs79500103	chr16:76443267-76443268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs62051219	chr16:76443298-76443299	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs182157801	chr16:76443328-76443329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537603829	chr16:76443353-76443354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554654477	chr16:76443361-76443362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs367648578	chr16:76443385-76443386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138047473	chr16:76443391-76443392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs553840191	chr16:76443426-76443427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs114531473	chr16:76443427-76443428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546531996	chr16:76443461-76443462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs111613318	chr16:76443464-76443465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556537109	chr16:76443473-76443474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs569666418	chr16:76443483-76443484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535382809	chr16:76443493-76443494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs562297317	chr16:76443516-76443517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568796801	chr16:76443534-76443535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34449971	chr16:76443550-76443551	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs565736459	chr16:76443616-76443617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541104138	chr16:76443619-76443620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140973943	chr16:76443629-76443630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs568083161	chr16:76443638-76443639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187167406	chr16:76443667-76443668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs74430927	chr16:76443673-76443674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369787060	chr16:76443699-76443700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531632709	chr16:76443718-76443719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs62051220	chr16:76443737-76443738	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs568232173	chr16:76443744-76443745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533905540	chr16:76443767-76443768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs145060747	chr16:76443774-76443775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs192096408	chr16:76443790-76443791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs539391567	chr16:76443797-76443798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556120076	chr16:76443800-76443801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs576957053	chr16:76443826-76443827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs369714972	chr16:76443837-76443838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs372469344	chr16:76443841-76443842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576704148	chr16:76443842-76443843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542492490	chr16:76443850-76443851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs555710930	chr16:76443865-76443866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs572277890	chr16:76443882-76443883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs183921442	chr16:76443916-76443917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs564200412	chr16:76443936-76443937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533159515	chr16:76443939-76443940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs138842277	chr16:76443955-76443956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs563693644	chr16:76443962-76443963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs375416371	chr16:76443971-76443972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs531534365	chr16:76444002-76444003	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
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
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76442600-76444600	Enhancers	Fetal Lung	lung

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