Variant report

Variant	nsv966497
Chromosome Location	chr4:97034860-97038396
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559000356	chr4:97035403-97035404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs149865778	chr4:97035436-97035437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574043213	chr4:97035463-97035464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114226329	chr4:97035485-97035486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs147590852	chr4:97035531-97035532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs117946001	chr4:97035547-97035548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545190490	chr4:97035558-97035559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs7695694	chr4:97035575-97035576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs187344964	chr4:97035596-97035597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115861111	chr4:97035601-97035602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191737246	chr4:97035636-97035637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183994807	chr4:97035692-97035693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551955265	chr4:97035694-97035695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs530052142	chr4:97035701-97035702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142116664	chr4:97035705-97035706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563496043	chr4:97035753-97035754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532298600	chr4:97035755-97035756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs17025073	chr4:97035768-97035769	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs565810745	chr4:97035787-97035788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534418011	chr4:97035792-97035793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534396056	chr4:97035829-97035830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548194251	chr4:97035864-97035865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555833247	chr4:97035885-97035886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188290442	chr4:97035936-97035937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs536560906	chr4:97035938-97035939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs180754795	chr4:97035948-97035949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs576231772	chr4:97035952-97035953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539182047	chr4:97035967-97035968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185613058	chr4:97035987-97035988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs190567489	chr4:97035994-97035995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181841807	chr4:97036023-97036024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555019973	chr4:97036050-97036051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574857319	chr4:97036125-97036126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs543743030	chr4:97036128-97036129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs375580006	chr4:97036173-97036174	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	19197363	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:97035400-97035800	Enhancers	Fetal Brain Male	brain
2	chr4:97035800-97036200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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