Variant report

Variant	nsv573083
Chromosome Location	chr16:77091028-77091809
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375084713	chr16:77091221-77091222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs149369933	chr16:77091249-77091250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559663127	chr16:77091254-77091255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs568555474	chr16:77091262-77091263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183215541	chr16:77091277-77091278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs77933502	chr16:77091282-77091283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532772115	chr16:77091286-77091287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147057913	chr16:77091421-77091422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138322064	chr16:77091428-77091429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs188178655	chr16:77091441-77091442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs368198934	chr16:77091450-77091451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537954144	chr16:77091459-77091460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1564928	chr16:77091472-77091473	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs574579227	chr16:77091496-77091497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574350739	chr16:77091508-77091509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs540459949	chr16:77091519-77091520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374754418	chr16:77091587-77091588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs9928199	chr16:77091611-77091612	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs568132999	chr16:77091625-77091626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192975926	chr16:77091627-77091628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs74025454	chr16:77091631-77091632	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs530773959	chr16:77091663-77091664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs530533128	chr16:77091668-77091669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556728449	chr16:77091693-77091694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532189271	chr16:77091694-77091695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561273549	chr16:77091695-77091696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530112840	chr16:77091697-77091698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546825208	chr16:77091809-77091810	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Lung cancer	24585490	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20581869	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
early-passage human iPS cells	21368824	CNVD
Melanoma	17363583	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:77091200-77097800	Enhancers	Primary neutrophils fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links